Template:Infobox drug/testcases#biosimilars
{{Testcases}}
{{Infobox drug/testcases/navbox|state=collapsed}}
biosimilars
:eg Rituximab
{{testcase table
|name=rituximab
|synonyms=synonyms
|biosimilars=rituximab-abbs,{{cite web | title=Truxima- rituximab-abbs injection, solution | website=DailyMed | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9af3ddc7-4217-417a-ac89-8704edc5bc44 | access-date=26 March 2021}} rituximab-pvvr,{{cite web | title=Ruxience- rituximab-pvvr injection, solution | website=DailyMed | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f941fc61-f7a3-4e4a-ab7c-87c1667fa05b | access-date=26 March 2021}} rituximab-arrx{{cite web | title=Riabni- rituximab-arrx injection, solution | website=DailyMed | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=da1c4de7-0e5b-4f72-97ec-7a8d368f085f | access-date=26 March 2021}}
|Drugs.com = {{drugs.com|monograph|rituximab}}
}}
{{Section references}}
Test Brazilian Legal Status
{{testcase table
| image =
| legal_status =
| legal_AU = S2
| legal_BR = A1
| legal_CA = Schedule I
| legal_DE = Anlage I
| legal_UK = GSL
| legal_US = Rx-only
}}
Test 0 = blanks
{{testcase table
| legal_status =
| legal_AU =
}}
Test 1
{{purge}}
{{testcase table
| name = {{PAGENAME}}
| INN = Linezolid
| Verifiedfields = changed
| verifiedrevid = 415028406
| IUPAC_name = (S)-N-({3-[3-fluoro-4-(morpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide
| image = Linezolid.svg
| alt = Skeletal formula of linezolid
| image2 = Linezolid-from-xtal-2008-3D-balls.png
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| tradename = Linospan, Zyvox, Zyvoxam, Zyvoxid
| Drugs.com = {{drugs.com|monograph|linezolid}}
| MedlinePlus = a602004
| licence_CA = Linezolid
| licence_EU = Linezolid
| DailyMedID = Linezolid
| licence_US = Linezolid
| pregnancy_US = C
| pregnancy_AU = C
| legal_status_AU = S4
| legal_status_UK = POM
| legal_status_US = ℞-only
| routes_of_administration = Intravenous infusion, oral
| dependency_liability = High
| addiction_liability = Low
| metabolites = some stuff
| duration_of_action= 1 to 3 hr
| bioavailability = ~100% (oral)
| protein_bound = Low (31%)
| metabolism = Hepatic (50–70%, CYP not involved)
| elimination_half-life = 4.2–5.4 hours (shorter in children)
| excretion = Nonrenal, renal, and fecal
| onset = 1 hr
| synonyms = Lenzomore
| CASNo_Ref = {{cascite|correct|CAS}}
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 165800-03-3
| ATC_prefix = J01
| ATC_suffix = XX08
| PubChem = 441401
| DrugBank_Ref =
| DrugBank = DB00601
| ChemSpiderID_Ref =
| ChemSpiderID =
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = ISQ9I6J12J
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D00947
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 126
| NIAID_ChemDB = 070944
| PDB_ligand = ZLD
| IUPHAR_ligand = 1234
| C=16 | H=20 | F=1 | N=3 | O=4
| molecular_weight = 337.346 g/mol
| smiles = O=C1O[C@@H](CNC(=O)C)CN1c3cc(F)c(N2CCOCC2)cc3
| InChI = 1/C16H20FN3O4/c1-11(21)18-9-13-10-20(16(22)24-13)12-2-3-15(14(17)8-12)19-4-6-23-7-5-19/h2-3,8,13H,4-7,9-10H2,1H3,(H,18,21)/t13-/m0/s1
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C16H20FN3O4/c1-11(21)18-9-13-10-20(16(22)24-13)12-2-3-15(14(17)8-12)19-4-6-23-7-5-19/h2-3,8,13H,4-7,9-10H2,1H3,(H,18,21)/t13-/m0/s1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = TYZROVQLWOKYKF-ZDUSSCGKSA-N
| density = 1.40
| melting_point = 135
| boiling_point = 140
| boiling_notes = (decomposes)
| solubility = 3}}
{{purge}}
Test 2
{{testcase table
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 401042653
| IUPAC_name = (7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z,26E)-26-{[(4-cyclopentylpiperazin-1-yl)amino]methylidene}-2,15,17,29-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23,27-trioxo-8,30-dioxa-24-azatetracyclo[23.3.1.14,7.05,28]triaconta-1(28),2,4,9,19,21,25(29)-heptaen-13-yl acetate
| image = Rifapentine.svg
| width = 250
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| tradename =
| Drugs.com = {{drugs.com|monograph|rifapentine}}
| MedlinePlus = a602026
| pregnancy_category =
| legal_status =
| routes_of_administration =
| bioavailability = increases when administered with food
| protein_bound =
| metabolism =
| elimination_half-life =
| onset = 1 hr
| CAS_number = 61379-65-5
| ATC_prefix = J04
| ATC_suffix = AB05
| ATC_supplemental =
| PubChem = 5462354
| DrugBank_Ref =
| DrugBank = APRD01217
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 10482075
| UNII_Ref = {{fdacite|changed|FDA}}
| UNII = XJM390A33U
| KEGG_Ref = {{keggcite|changed|kegg}}
| KEGG = D00879
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 45304
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 1660
| NIAID_ChemDB = 007686
| C=47 | H=64 | N=4 | O=12
| molecular_weight = 877.031 g/mol
| smiles = CC(=O)O[C@H]3[C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(\C)C(=O)Nc6c(/C=N/N1CCN(CC1)C2CCCC2)c(O)c5c4C(=O)[C@@](C)(O/C=C/[C@H](OC)[C@H]3C)Oc4c(C)c(O)c5c6O
| InChI = 1/C47H64N4O12/c1-24-13-12-14-25(2)46(59)49-37-32(23-48-51-20-18-50(19-21-51)31-15-10-11-16-31)41(56)34-35(42(37)57)40(55)29(6)44-36(34)45(58)47(8,63-44)61-22-17-33(60-9)26(3)43(62-30(7)52)28(5)39(54)27(4)38(24)53/h12-14,17,22-24,26-28,31,33,38-39,43,53-57H,10-11,15-16,18-21H2,1-9H3,(H,49,59)/b13-12+,22-17+,25-14-,48-23+/t24-,26+,27+,28+,33-,38-,39+,43+,47-/m0/s1
| InChIKey = WDZCUPBHRAEYDL-GZAUEHORBZ
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C47H64N4O12/c1-24-13-12-14-25(2)46(59)49-37-32(23-48-51-20-18-50(19-21-51)31-15-10-11-16-31)41(56)34-35(42(37)57)40(55)29(6)44-36(34)45(58)47(8,63-44)61-22-17-33(60-9)26(3)43(62-30(7)52)28(5)39(54)27(4)38(24)53/h12-14,17,22-24,26-28,31,33,38-39,43,53-57H,10-11,15-16,18-21H2,1-9H3,(H,49,59)/b13-12+,22-17+,25-14-,48-23+/t24-,26+,27+,28+,33-,38-,39+,43+,47-/m0/s1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = WDZCUPBHRAEYDL-GZAUEHORSA-N
| StdInChIKey_comment = Some comment StdInChIkey here
| StdInChI_comment = Commenting hereHello world
| synonyms = 3{[(4-cyclopentyl-1-piperazinyl)imino]methyl}rifamycin
}}
{{Section references}}
Test 3
{{testcase table
| image =
| type = vaccine
| target = Tuberculosis
| vaccine_type = live
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| Drugs.com = {{drugs.com|pro|bcg-vaccine}}
| pregnancy_AU =
| pregnancy_US = C
| pregnancy_category =
| legal_AU =
| legal_CA =
| legal_UK =
| legal_US = Rx-only
| legal_status =
| routes_of_administration = Percutaneous
| CAS_number =
| ATC_prefix = J07
| ATC_suffix = AN01
| PubChem =
| DrugBank =
| ChemSpiderID = NA
}}
Test 4
{{testcase table
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 477861573
| name = Atorvastatin
| IUPAC_name = (3R,5R)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-propan-2-ylpyrrol-1-yl]-3,5-dihydroxyheptanoic acid
| image = Atorvastatin2DCSD.svg
| width = 300
| image2 = Atorvastatin3Dan.gif
| width2 = 250
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| tradename = Lipitor, Atorva
| Drugs.com = {{drugs.com|monograph|lipitor}}
| MedlinePlus = a600045
| licence_US = Atorvastatin
| pregnancy_AU = D
| pregnancy_US = X
| legal_AU = S4
| legal_UK = POM
| legal_US = Rx-only
| routes_of_administration = Oral
| DailyMedID = 42465
| bioavailability = 12%
| metabolism = Hepatic - CYP3A4
| elimination_half-life = 14 h
| excretion = Bile
| onset = 1 hr
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 134523-00-5
| ATC_prefix = C10
| ATC_suffix = AA05
| PubChem = 60823
| DrugBank_Ref = {{drugbankcite|changed|drugbank}}
| DrugBank = APRD00055
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 54810
| UNII_Ref = {{fdacite|changed|FDA}}
| UNII = A0JWA85V8F
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D07474
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 39548
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1487
| PDB_ligand = 117
| IUPHAR_ligand = 2949
| C=33 | H=35 | F=1 | N=2| Ca=2 | O=5
| molecular_weight = 558.64
| smiles = O=C(O)C[C@H](O)C[C@H](O)CCn2c(c(c(c2c1ccc(F)cc1)c3ccccc3)C(=O)Nc4ccccc4)C(C)C
| InChI = 1/C33H35FN2O5/c1-21(2)31-30(33(41)35-25-11-7-4-8-12-25)29(22-9-5-3-6-10-22)32(23-13-15-24(34)16-14-23)36(31)18-17-26(37)19-27(38)20-28(39)40/h3-16,21,26-27,37-38H,17-20H2,1-2H3,(H,35,41)(H,39,40)/t26-,27-/m1/s1
| InChIKey = XUKUURHRXDUEBC-KAYWLYCHBX
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C33H35FN2O5/c1-21(2)31-30(33(41)35-25-11-7-4-8-12-25)29(22-9-5-3-6-10-22)32(23-13-15-24(34)16-14-23)36(31)18-17-26(37)19-27(38)20-28(39)40/h3-16,21,26-27,37-38H,17-20H2,1-2H3,(H,35,41)(H,39,40)/t26-,27-/m1/s1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = XUKUURHRXDUEBC-KAYWLYCHSA-N
}}
Test all 1
{{Testcase table
| drug_name = 1
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| imagename = 2
| type = 3
| name = testcases
| image = Simple shapes example.png
| width = 175px
| alt = an example image
| image2 = Nocover.svg
| width2 = 150px
| alt2 = another example image
| caption = some images
| IUPAC_name = 12
| target = 13
| vaccine_type = Toxoid
| mab_type = F(ab')2
| source = xi/a
| component1 = 17
| class1 = 18
| component2 = 19
| class2 = 20
| component3 = 21
| class3 = 22
| component4 = 23
| class4 = 24
| tradename = 25
| ASHP = 26
| Drugs.com = 27
| eMedicine = 28
| MedlinePlus = 29
| licence_EU = 30
| licence_US = 31
| DailyMedID = 32
| pregnancy_AU = B3
| pregnancy_US = C
| pregnancy_category = 35
| legal_AU = S4
| legal_CA = Schedule IV
| legal_UK = POM
| legal_US = Schedule III
| legal_UN = N II III
| legal_EU = Category 2 Precursor
| legal_status = RX
| dependency_liability = 43
| routes_of_administration = 44
| bioavailability = 45
| protein_bound = 46
| metabolism = 47
| onset = 47.5
| elimination_half-life = 48
| excretion = 49
| CAS_number = 50
| CAS_number_Ref = 51
| CAS_supplemental = 52
| ATCvet = 53
| ATC_prefix = 54
| ATC_suffix = 55
| ATC_supplemental = 56
| PubChem = 57
| PubChemSubstance = 58
| IUPHAR_ligand = 59
| DrugBank = 60
| ChemSpiderID = 61
| ChemSpiderID_Ref = 62
| UNII = 63
| UNII_Ref = 64
| KEGG = 65
| KEGG_Ref = 66
| ChEBI = 67
| ChEBI_Ref = 68
| ChEMBL = 69
| ChEMBL_Ref = 70
| NIAID_ChemDB = 71
| synonyms = 72
| PDB_ligand = 73
| chemical_formula = 74
| C = 1
| H = 2
| Ag = 3
| Al = 4
| As = 5
| Au = 6
| B = 7
| Bi = 8
| Br = 9
| Ca = 10
| Cl = 11
| Co = 12
| Cr = 13
| F = 14
| Fe = 15
| Gd = 16
| Hg = 17
| I = 18
| K = 19
| Li = 20
| Mg = 21
| Mn = 22
| N = 23
| Na = 24
| O = 25
| P = 26
| Pt = 27
| S = 28
| Sb = 29
| Se = 30
| Si = 31
| Sr = 32
| Tc = 33
| Zn = 34
| charge = -1
| molecular_weight = 75
| smiles = 76
| StdInChI = 77
| StdInChI_comment = 78
| StdInChI_Ref = 79
| StdInChIKey = 80
| StdInChIKey_comment = 81
| StdInChIKey_Ref = 82
| density = 83
| density_notes = note83
| melting_point = 84
| melting_high = 85
| melting_notes = 86
| boiling_point = 87
| boiling_notes = 88
| solubility = 89
| specific_rotation = 90
| sec_combustion = 91
| Verifiedfields = 92
| verifiedrevid = 93
}}
Test all 2
{{Testcase table
| drug_name = 1
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| imagename = 2
| type = combo
| name = testcases
| image = Simple shapes example.png
| width = 175px
| alt = an example image
| image2 = Nocover.svg
| width2 = 150px
| alt2 = another example image
| caption = some images
| IUPAC_name = 12
| target = 13
| vaccine_type = Toxoid
| mab_type = F(ab')2
| source = xi/a
| component1 = 17
| class1 = 18
| component2 = 19
| class2 = 20
| component3 = 21
| class3 = 22
| component4 = 23
| class4 = 24
| tradename = 25
| ASHP = 26
| Drugs.com = 27
| eMedicine = 28
| MedlinePlus = 29
| licence_EU = 30
| licence_US = 31
| DailyMedID = 32
| pregnancy_AU = B3
| pregnancy_US = C
| pregnancy_category = 35
| legal_AU = S4
| legal_CA = Schedule IV
| legal_UK = POM
| legal_US = Schedule III
| legal_UN = N II III
| legal_EU = Category 2 Precursor
| legal_status = RX
| dependency_liability = 43
| routes_of_administration = 44
| bioavailability = 45
| protein_bound = 46
| metabolism = 47
| onset = 47.5
| elimination_half-life = 48
| excretion = 49
| CAS_number = 50
| CAS_number_Ref = 51
| CAS_supplemental = 52
| ATCvet = 53
| ATC_prefix = 54
| ATC_suffix = 55
| ATC_supplemental = 56
| PubChem = 57
| PubChemSubstance = 58
| IUPHAR_ligand = 59
| DrugBank = 60
| ChemSpiderID = 61
| ChemSpiderID_Ref = 62
| UNII = 63
| UNII_Ref = 64
| KEGG = 65
| KEGG_Ref = 66
| ChEBI = 67
| ChEBI_Ref = 68
| ChEMBL = 69
| ChEMBL_Ref = 70
| NIAID_ChemDB = 71
| synonyms = 72
| PDB_ligand = 73
| chemical_formula = 74
| C = 1
| H = 2
| Ag = 3
| Al = 4
| As = 5
| Au = 6
| B = 7
| Bi = 8
| Br = 9
| Ca = 10
| Cl = 11
| Co = 12
| Cr = 13
| F = 14
| Fe = 15
| Gd = 16
| Hg = 17
| I = 18
| K = 19
| Li = 20
| Mg = 21
| Mn = 22
| N = 23
| Na = 24
| O = 25
| P = 26
| Pt = 27
| S = 28
| Sb = 29
| Se = 30
| Si = 31
| Sr = 32
| Tc = 33
| Zn = 34
| charge = -1
| molecular_weight = 75
| smiles = 76
| StdInChI = 77
| StdInChI_comment = 78
| StdInChI_Ref = 79
| StdInChIKey = 80
| StdInChIKey_comment = 81
| StdInChIKey_Ref = 82
| density = 83
| melting_point = 84
| melting_high = 85
| melting_notes = 86
| boiling_point = 87
| boiling_notes = 88
| solubility = 89
| specific_rotation = 90
| sec_combustion = 91
| Verifiedfields = 92
| verifiedrevid = 93
}}
Test all 3
{{Testcase table
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| drug_name = 1
| imagename = 2
| type = vaccine
| name = testcases
| image = Simple shapes example.png
| width = 175px
| alt = an example image
| image2 = Nocover.svg
| width2 = 150px
| alt2 = another example image
| caption = some images
| IUPAC_name = 12
| target = 13
| vaccine_type = Toxoid
| mab_type = F(ab')2
| source = xi/a
| component1 = 17
| class1 = 18
| component2 = 19
| class2 = 20
| component3 = 21
| class3 = 22
| component4 = 23
| class4 = 24
| tradename = 25
| ASHP = 26
| Drugs.com = 27
| eMedicine = 28
| MedlinePlus = 29
| licence_EU = 30
| licence_US = 31
| DailyMedID = 32
| pregnancy_AU = B3
| pregnancy_US = C
| pregnancy_category = 35
| legal_AU = S4
| legal_CA = Schedule IV
| legal_UK = POM
| legal_US = Schedule III
| legal_UN = N II III
| legal_EU = Category 2 Precursor
| legal_status = RX
| dependency_liability = 43
| routes_of_administration = 44
| bioavailability = 45
| protein_bound = 46
| metabolism = 47
| onset = 47.5
| elimination_half-life = 48
| excretion = 49
| CAS_number = 50
| CAS_number_Ref = 51
| CAS_supplemental = 52
| ATCvet = 53
| ATC_prefix = 54
| ATC_suffix = 55
| ATC_supplemental = 56
| PubChem = 57
| PubChemSubstance = 58
| IUPHAR_ligand = 59
| DrugBank = 60
| ChemSpiderID = 61
| ChemSpiderID_Ref = 62
| UNII = 63
| UNII_Ref = 64
| KEGG = 65
| KEGG_Ref = 66
| ChEBI = 67
| ChEBI_Ref = 68
| ChEMBL = 69
| ChEMBL_Ref = 70
| NIAID_ChemDB = 71
| synonyms = 72
| PDB_ligand = 73
| chemical_formula = 74
| C = 1
| H = 2
| Ag = 3
| Al = 4
| As = 5
| Au = 6
| B = 7
| Bi = 8
| Br = 9
| Ca = 10
| Cl = 11
| Co = 12
| Cr = 13
| F = 14
| Fe = 15
| Gd = 16
| Hg = 17
| I = 18
| K = 19
| Li = 20
| Mg = 21
| Mn = 22
| N = 23
| Na = 24
| O = 25
| P = 26
| Pt = 27
| S = 28
| Sb = 29
| Se = 30
| Si = 31
| Sr = 32
| Tc = 33
| Zn = 34
| charge = -1
| molecular_weight = 75
| smiles = 76
| StdInChI = 77
| StdInChI_comment = 78
| StdInChI_Ref = 79
| StdInChIKey = 80
| StdInChIKey_comment = 81
| StdInChIKey_Ref = 82
| density = 83
| melting_point = 84
| melting_high = 85
| melting_notes = 86
| boiling_point = 87
| boiling_notes = 88
| solubility = 89
| specific_rotation = 90
| sec_combustion = 91
| Verifiedfields = 92
| verifiedrevid = 93
}}
Test all 4
{{Testcase table
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| drug_name = 1
| imagename = 2
| type = mab
| name = testcases
| image = Simple shapes example.png
| width = 175px
| alt = an example image
| image2 = Nocover.svg
| width2 = 150px
| alt2 = another example image
| caption = some images
| IUPAC_name = 12
| target = 13
| vaccine_type = Toxoid
| mab_type = F(ab')2
| source = xi/a
| component1 = 17
| class1 = 18
| component2 = 19
| class2 = 20
| component3 = 21
| class3 = 22
| component4 = 23
| class4 = 24
| tradename = 25
| ASHP = 26
| Drugs.com = 27
| eMedicine = 28
| MedlinePlus = 29
| licence_EU = 30
| licence_US = 31
| DailyMedID = 32
| pregnancy_AU = B3
| pregnancy_US = C
| pregnancy_category = 35
| legal_AU = S4
| legal_CA = Schedule IV
| legal_UK = POM
| legal_US = Schedule III
| legal_UN = N II III
| legal_EU = Category 2 Precursor
| legal_status = RX
| dependency_liability = 43
| addiction_liability = 43b
| routes_of_administration = 44
| bioavailability = 45
| protein_bound = 46
| metabolism = 47
| onset = 47.5
| elimination_half-life = 48
| excretion = 49
| CAS_number = 50
| CAS_number_Ref = 51
| CAS_supplemental = 52
| ATCvet = 53
| ATC_prefix = 54
| ATC_suffix = 55
| ATC_supplemental = 56
| PubChem = 57
| PubChemSubstance = 58
| IUPHAR_ligand = 59
| DrugBank = 60
| ChemSpiderID = 61
| ChemSpiderID_Ref = 62
| UNII = 63
| UNII_Ref = 64
| KEGG = 65
| KEGG_Ref = 66
| ChEBI = 67
| ChEBI_Ref = 68
| ChEMBL = 69
| ChEMBL_Ref = 70
| NIAID_ChemDB = 71
| synonyms = 72
| PDB_ligand = 73
| chemical_formula = 74
| C = 1
| H = 2
| Ag = 3
| Al = 4
| As = 5
| Au = 6
| B = 7
| Bi = 8
| Br = 9
| Ca = 10
| Cl = 11
| Co = 12
| Cr = 13
| F = 14
| Fe = 15
| Gd = 16
| Hg = 17
| I = 18
| K = 19
| Li = 20
| Mg = 21
| Mn = 22
| N = 23
| Na = 24
| O = 25
| P = 26
| Pt = 27
| S = 28
| Sb = 29
| Se = 30
| Si = 31
| Sr = 32
| Tc = 33
| Zn = 34
| charge = -1
| molecular_weight = 75
| smiles = 76
| StdInChI = 77
| StdInChI_comment = 78
| StdInChI_Ref = 79
| StdInChIKey = 80
| StdInChIKey_comment = 81
| StdInChIKey_Ref = 82
| density = 83
| melting_point = 84
| melting_high = 85
| melting_notes = 86
| boiling_point = 87
| boiling_notes = 88
| solubility = 89
| specific_rotation = 90
| sec_combustion = 91
| Verifiedfields = 92
| verifiedrevid = 93
}}
Test formula 1
{{Testcase table
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| drug_name = 1
| imagename = 2
| type = 3
| name = testcases
| image = Simple shapes example.png
| width = 175px
| alt = an example image
| image2 = Nocover.svg
| width2 = 150px
| alt2 = another example image
| caption = some images
| IUPAC_name = 12
| target = 13
| vaccine_type = Toxoid
| mab_type = F(ab')2
| source = xi/a
| component1 = 17
| class1 = 18
| component2 = 19
| class2 = 20
| component3 = 21
| class3 = 22
| component4 = 23
| class4 = 24
| tradename = 25
| ASHP = 26
| Drugs.com = 27
| eMedicine = 28
| MedlinePlus = 29
| licence_EU = 30
| licence_US = 31
| DailyMedID = 32
| pregnancy_AU = B3
| pregnancy_US = C
| pregnancy_category = 35
| legal_AU = S4
| legal_CA = Schedule IV
| legal_UK = POM
| legal_US = Schedule III
| legal_UN = N II III
| legal_EU = Category 2 Precursor
| legal_status = RX
| dependency_liability = 43
| routes_of_administration = 44
| bioavailability = 45
| protein_bound = 46
| metabolism = 47
| onset = 47.5
| elimination_half-life = 48
| excretion = 49
| CAS_number = 50
| CAS_number_Ref = 51
| CAS_supplemental = 52
| ATCvet = 53
| ATC_prefix = 54
| ATC_suffix = 55
| ATC_supplemental = 56
| PubChem = 57
| PubChemSubstance = 58
| IUPHAR_ligand = 59
| DrugBank = 60
| ChemSpiderID = 61
| ChemSpiderID_Ref = 62
| UNII = 63
| UNII_Ref = 64
| KEGG = 65
| KEGG_Ref = 66
| ChEBI = 67
| ChEBI_Ref = 68
| ChEMBL = 69
| ChEMBL_Ref = 70
| NIAID_ChemDB = 71
| synonyms = 72
| PDB_ligand = 73
| chemical_formula =
| C = 1
| H = 2
| Ag = 3
| Al = 4
| As = 5
| Au = 6
| B = 7
| Bi = 8
| charge = -1
| molecular_weight = 75
| smiles = 76
| StdInChI = 77
| StdInChI_comment = 78
| StdInChI_Ref = 79
| StdInChIKey = 80
| StdInChIKey_comment = 81
| StdInChIKey_Ref = 82
| density = 83
| melting_point = 84
| melting_high = 85
| melting_notes = 86
| boiling_point = 87
| boiling_notes = 88
| solubility = 89
| specific_rotation = 90
| sec_combustion = 91
| Verifiedfields = 92
| verifiedrevid = 93
}}
Test formula 2
{{Testcase table
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| drug_name = 1
| imagename = 2
| type = 3
| name = testcases
| image = Simple shapes example.png
| width = 175px
| alt = an example image
| image2 = Nocover.svg
| width2 = 150px
| alt2 = another example image
| caption = some images
| IUPAC_name = 12
| target = 13
| vaccine_type = Toxoid
| mab_type = F(ab')2
| source = xi/a
| component1 = 17
| class1 = 18
| component2 = 19
| class2 = 20
| component3 = 21
| class3 = 22
| component4 = 23
| class4 = 24
| tradename = 25
| ASHP = 26
| Drugs.com = 27
| eMedicine = 28
| MedlinePlus = 29
| licence_EU = 30
| licence_US = 31
| DailyMedID = 32
| pregnancy_AU = B3
| pregnancy_US = C
| pregnancy_category = 35
| legal_AU = S4
| legal_CA = Schedule IV
| legal_UK = POM
| legal_US = Schedule III
| legal_UN = N II III
| legal_EU = Category 2 Precursor
| legal_status = RX
| dependency_liability = 43
| routes_of_administration = 44
| bioavailability = 45
| protein_bound = 46
| metabolism = 47
| onset = 47.5
| elimination_half-life = 48
| excretion = 49
| CAS_number = 50
| CAS_number_Ref = 51
| CAS_supplemental = 52
| ATCvet = 53
| ATC_prefix = 54
| ATC_suffix = 55
| ATC_supplemental = 56
| PubChem = 57
| PubChemSubstance = 58
| IUPHAR_ligand = 59
| DrugBank = 60
| ChemSpiderID = 61
| ChemSpiderID_Ref = 62
| UNII = 63
| UNII_Ref = 64
| KEGG = 65
| KEGG_Ref = 66
| ChEBI = 67
| ChEBI_Ref = 68
| ChEMBL = 69
| ChEMBL_Ref = 70
| NIAID_ChemDB = 71
| synonyms = 72
| PDB_ligand = 73
| chemical_formula =
| C = 1
| Br = 9
| Ca = 10
| Cl = 11
| Co = 12
| Cr = 13
| F = 14
| Fe = 15
| Gd = 16
| Hg = 17
| charge = -1
| molecular_weight = 75
| smiles = 76
| StdInChI = 77
| StdInChI_comment = 78
| StdInChI_Ref = 79
| StdInChIKey = 80
| StdInChIKey_comment = 81
| StdInChIKey_Ref = 82
| density_notes = note83
| melting_point = 84
| melting_high = 85
| melting_notes = 86
| boiling_point = 87
| boiling_notes = 88
| solubility = 89
| specific_rotation = 90
| sec_combustion = 91
| Verifiedfields = 92
| verifiedrevid = 93
}}
Test formula 3
{{Testcase table
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| drug_name = 1
| imagename = 2
| type = 3
| name = testcases
| image = Simple shapes example.png
| width = 175px
| alt = an example image
| image2 = Nocover.svg
| width2 = 150px
| alt2 = another example image
| caption = some images
| IUPAC_name = 12
| target = 13
| vaccine_type = Toxoid
| mab_type = F(ab')2
| source = xi/a
| component1 = 17
| class1 = 18
| component2 = 19
| class2 = 20
| component3 = 21
| class3 = 22
| component4 = 23
| class4 = 24
| tradename = 25
| ASHP = 26
| Drugs.com = 27
| eMedicine = 28
| MedlinePlus = 29
| licence_EU = 30
| licence_US = 31
| DailyMedID = 32
| pregnancy_AU = B3
| pregnancy_US = C
| pregnancy_category = 35
| legal_AU = S4
| legal_CA = Schedule IV
| legal_UK = POM
| legal_US = Schedule III
| legal_UN = N II III
| legal_EU = Category 2 Precursor
| legal_status = RX
| dependency_liability = 43
| routes_of_administration = 44
| bioavailability = 45
| protein_bound = 46
| metabolism = 47
| onset = 47.5
| elimination_half-life = 48
| excretion = 49
| CAS_number = 50
| CAS_number_Ref = 51
| CAS_supplemental = 52
| ATCvet = 53
| ATC_prefix = 54
| ATC_suffix = 55
| ATC_supplemental = 56
| PubChem = 57
| PubChemSubstance = 58
| IUPHAR_ligand = 59
| DrugBank = 60
| ChemSpiderID = 61
| ChemSpiderID_Ref = 62
| UNII = 63
| UNII_Ref = 64
| KEGG = 65
| KEGG_Ref = 66
| ChEBI = 67
| ChEBI_Ref = 68
| ChEMBL = 69
| ChEMBL_Ref = 70
| NIAID_ChemDB = 71
| synonyms = 72
| PDB_ligand = 73
| chemical_formula =
| I = 18
| K = 19
| Li = 20
| Mg = 21
| Mn = 22
| N = 23
| Na = 24
| O = 25
| P = 26
| Pt = 27
| charge = -1
| molecular_weight = 75
| smiles = 76
| StdInChI = 77
| StdInChI_comment = 78
| StdInChI_Ref = 79
| StdInChIKey = 80
| StdInChIKey_comment = 81
| StdInChIKey_Ref = 82
| density = 83
| melting_point = 84
| melting_high = 85
| melting_notes = 86
| boiling_point = 87
| boiling_notes = 88
| solubility = 89
| specific_rotation = 90
| sec_combustion = 91
| Verifiedfields = 92
| verifiedrevid = 93
}}
Test formula 4
{{Testcase table
| pronounce = {{IPAc-en|nj|uː|ˈ|m|əʊ|n|i|ə}}
| drug_name = 1
| imagename = 2
| type = 3
| name = testcases
| image = Simple shapes example.png
| width = 175px
| alt = an example image
| image2 = Nocover.svg
| width2 = 150px
| alt2 = another example image
| caption = some images
| IUPAC_name = 12
| target = 13
| vaccine_type = Toxoid
| mab_type = F(ab')2
| source = xi/a
| component1 = 17
| class1 = 18
| component2 = 19
| class2 = 20
| component3 = 21
| class3 = 22
| component4 = 23
| class4 = 24
| tradename = 25
| ASHP = 26
| Drugs.com = 27
| eMedicine = 28
| MedlinePlus = 29
| licence_EU = 30
| licence_US = 31
| DailyMedID = 32
| pregnancy_AU = B3
| pregnancy_US = C
| pregnancy_category = 35
| legal_AU = S4
| legal_CA = Schedule IV
| legal_UK = POM
| legal_US = Schedule III
| legal_UN = N II III
| legal_EU = Category 2 Precursor
| legal_status = RX
| dependency_liability = 43
| routes_of_administration = 44
| bioavailability = 45
| protein_bound = 46
| metabolism = 47
| onset = 47.5
| elimination_half-life = 48
| excretion = 49
| CAS_number = 50
| CAS_number_Ref = 51
| CAS_supplemental = 52
| ATCvet = 53
| ATC_prefix = 54
| ATC_suffix = 55
| ATC_supplemental = 56
| PubChem = 57
| PubChemSubstance = 58
| IUPHAR_ligand = 59
| DrugBank = 60
| ChemSpiderID = 61
| ChemSpiderID_Ref = 62
| UNII = 63
| UNII_Ref = 64
| KEGG = 65
| KEGG_Ref = 66
| ChEBI = 67
| ChEBI_Ref = 68
| ChEMBL = 69
| ChEMBL_Ref = 70
| NIAID_ChemDB = 71
| synonyms = 72
| PDB_ligand = 73
| chemical_formula =
| S = 28
| Sb = 29
| Se = 30
| Si = 31
| Sr = 32
| Tc = 33
| Zn = 34
| charge = -1
| molecular_weight = 75
| smiles = 76
| StdInChI = 77
| StdInChI_comment = 78
| StdInChI_Ref = 79
| StdInChIKey = 80
| StdInChIKey_comment = 81
| StdInChIKey_Ref = 82
| density = 83
| melting_point = 84
| melting_high = 85
| melting_notes = 86
| boiling_point = 87
| boiling_notes = 88
| solubility = 89
| specific_rotation = 90
| sec_combustion = 91
| Verifiedfields = 92
| verifiedrevid = 93
}}
Legal status in the US
{{Testcase table
| verifiedrevid = 456481815
| image = Fluoxetine.svg
| image_class = skin-invert-image
| width =
| alt =
| image2 = R-and-S-fluoxetine-enantiomers-based-on-HCl-xtal-Mercury-3D-balls.png
| image_class2 = bg-transparent
| width2 = 250
| alt2 =
| caption = Fluoxetine (top),
(R)-fluoxetine (left), (S)-fluoxetine (right)
| chirality = Racemic mixture
|pronounce = US: {{IPAc-en|f|l|u|ˈ|ɑː|k|s|ə|t|iː|n}} {{respell|floo|AHKS|ə|teen}}
UK: {{IPAc-en|f|l|u|ˈ|ɒ|k|s|ə|t|iː|n}} {{respell|floo|OKS|ə|teen}}
| tradename = Prozac, Sarafem, others
| Drugs.com = {{drugs.com|monograph|fluoxetine-hydrochloride}}
| MedlinePlus = a689006
| DailyMedID = Fluoxetine
| pregnancy_AU = C
| pregnancy_AU_comment =
| pregnancy_category =
| dependency_liability =
| addiction_liability = None{{cite book |vauthors = Hubbard JR, Martin PR |title= Substance Abuse in the Mentally and Physically Disabled |date=2001 |publisher=CRC Press |isbn=978-0-8247-4497-7 |page=26 |url=https://books.google.com/books?id=MY1kFYk98mQC&pg=PA26 }}
| routes_of_administration = By mouth
| class = Selective serotonin reuptake inhibitor (SSRI)
| ATC_prefix = N06
| ATC_suffix = AB03
| ATC_supplemental = {{ATCvet|N06|AB03}}
| legal_AU = S4
| legal_AU_comment =
| legal_BR = C1
| legal_BR_comment =
| legal_CA = Rx-only
| legal_CA_comment =
| legal_DE =
| legal_DE_comment =
| legal_NZ =
| legal_NZ_comment =
| legal_UK = POM
| legal_UK_comment =
| legal_US = Rx-only
| legal_US_comment =
| legal_EU = Rx-only
| legal_EU_comment =
| legal_UN =
| legal_UN_comment =
| legal_status =
| bioavailability = 60–80%
| protein_bound = 94–95%
| metabolism = Liver (mostly CYP2D6-mediated)
| metabolites = Norfluoxetine, desmethylfluoxetine
| onset =
| elimination_half-life = 1–3 days (acute)
4–6 days (chronic)
| duration_of_action =
| excretion = Urine (80%), faeces (15%){{cite web|title=Prozac Fluoxetine Hydrochloride|work=TGA eBusiness Services|publisher=Eli Lilly Australia Pty. Limited|date=9 October 2013|access-date=23 November 2013|url=https://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent&id=CP-2010-PI-04098-3|format=PDF|url-status=live|archive-url=https://web.archive.org/web/20170425231029/https://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent&id=CP-2010-PI-04098-3|archive-date=25 April 2017}}{{cite journal |vauthors = Altamura AC, Moro AR, Percudani M |title = Clinical pharmacokinetics of fluoxetine |journal = Clinical Pharmacokinetics |volume = 26 |issue = 3 |pages = 201–14 |date = March 1994 |pmid = 8194283 |doi = 10.2165/00003088-199426030-00004 |s2cid = 1406955 }}
|index2_label = as HCl
| CAS_number_Ref = {{cascite|correct|CAS}}
| CAS_number = 54910-89-3
| CAS_number2_Ref = {{cascite|correct|CAS}}
| CAS_number2 = 56296-78-7
| CAS_supplemental =
| PubChem = 3386
| PubChem2 = 62857
| IUPHAR_ligand = 203
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = DB00472
| DrugBank2_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank2 = DBSALT000087
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 3269
| ChemSpiderID2_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID2 = 56589
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 01K63SUP8D
| UNII2_Ref = {{fdacite|correct|FDA}}
| UNII2 = I9W7N6B1KJ
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D00326
| KEGG2_Ref = {{keggcite|correct|kegg}}
| KEGG2 = D00823
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 5118
| ChEBI2_Ref = {{ebicite|correct|EBI}}
| ChEBI2 = 5119
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 41
| ChEMBL2_Ref = {{ebicite|correct|EBI}}
| ChEMBL2 = 1201082
| NIAID_ChemDB =
| PDB_ligand =
| synonyms =
| IUPAC_name = N-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine
| C = 17
| H = 18
| F = 3
| N = 1
| O = 1
| SMILES = CNCCC(c1ccccc1)Oc2ccc(cc2)C(F)(F)F
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C17H18F3NO/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20/h2-10,16,21H,11-12H2,1H3
| StdInChI_comment =
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = RTHCYVBBDHJXIQ-UHFFFAOYSA-N
| density =
| density_notes =
| melting_point = 179
| melting_high = 182
| melting_notes =
| boiling_point = 395
| boiling_notes =
| solubility = 14
| sol_units =
| specific_rotation =
}}