Sulfacetamide
Blephamide, Cetapred, Fml-s, Gyne-sulf, Klaron, Metimyd, Predamide, Predsulfair, Sulphrin, Sulster, Sultrin, Trysul, Vagilia, Vasocidin (sulfacetamide) is a small molecule pharmaceutical. Sulfacetamide was first approved as Blephamide on 1982-01-01. It is used to treat bacterial infections, bacterial skin diseases, corneal ulcer, ear diseases, and seborrheic dermatitis amongst others in the USA.
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Commercial
Trade Name
FDA
EMA
Klaron (generic drugs available since 1982-01-01, discontinued: Bleph, Cetamide, Isopto cetamide, Ocusulf, Sulamyd, Sulf, Sulfacel, Sulfair, Sulten)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Fluorometholone
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Sulfacetamide sodium
Tradename | Company | Number | Date | Products |
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FML-S | Allergan | N-019525 DISCN | 1989-09-29 | 1 products |
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Prednisolone acetate
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Sulfacetamide sodium
Prednisolone sodium phosphate
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Sulfacetamide sodium
Tradename | Company | Number | Date | Products |
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VASOCIDIN | Novartis | N-018988 DISCN | 1988-08-26 | 1 products, RLD |
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Sulfacetamide sodium
Tradename | Company | Number | Date | Products |
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KLARON | Bausch Health Companies | N-019931 RX | 1996-12-23 | 1 products, RLD, RS |
Show 1 discontinued
Sulfacetamide
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Sulfathiazole)
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Triple sulfa (sulfabenzamide
Tradename | Company | Number | Date | Products |
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SULTRIN | Johnson & Johnson | N-005794 DISCN | 1982-01-01 | 2 products |
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Labels
FDA
EMA
Brand Name | Status | Last Update |
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blephamide | New Drug Application | 2013-11-15 |
cetamide isopto cetamide | 2006-11-20 | |
fml-s | 2007-02-20 | |
klaron | New Drug Application | 2020-08-31 |
sulfacetamide sodium | ANDA | 2023-06-07 |
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
D: Dermatologicals
— D10: Anti-acne preparations
— D10A: Anti-acne preparations for topical use
— D10AF: Antiinfectives for treatment of acne
— D10AF06: Sulfacetamide
S: Sensory organ drugs
— S01: Ophthalmologicals
— S01A: Antiinfective ophthalmologics
— S01AB: Sulfonamides, ophthalmologic antiinfectives
— S01AB04: Sulfacetamide
HCPCS
No data
Clinical
Clinical Trials
10 clinical trials
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Indications Phases 4
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Indications Phases 3
No data
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Hypertrophic cardiomyopathy | D002312 | EFO_0000538 | I42.1 | 1 | 2 | — | — | — | 3 |
Dilated cardiomyopathy | D002311 | EFO_0000407 | I42.0 | 2 | 1 | — | — | — | 2 |
Heart failure | D006333 | EFO_0003144 | I50 | 1 | 1 | — | — | — | 1 |
Ventricular outflow obstruction | D014694 | EFO_1001448 | — | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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Healthy volunteers/patients | — | 5 | — | — | — | — | 5 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | SULFACETAMIDE |
INN | sulfacetamide |
Description | Sulfacetamide is a sulfonamide that is sulfanilamide acylated on the sulfonamide nitrogen. It has a role as an antimicrobial agent, an antiinfective agent, an EC 2.5.1.15 (dihydropteroate synthase) inhibitor and an antibacterial drug. It is a substituted aniline and a N-sulfonylcarboxamide. It is functionally related to a sulfanilamide. It is a conjugate acid of a sulfacetamide(1-). |
Classification | Small molecule |
Drug class | antimicrobials (sulfonamides derivatives) |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | CC(=O)NS(=O)(=O)c1ccc(N)cc1 |
Identifiers
PDB | — |
CAS-ID | 144-80-9 |
RxCUI | 10169 |
ChEMBL ID | CHEMBL455 |
ChEBI ID | 63845 |
PubChem CID | 5320 |
DrugBank | DB00634 |
UNII ID | 4965G3J0F5 (ChemIDplus, GSRS) |
Target
Agency Approved
No data
Alternate
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Variants
Clinical Variant
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Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 895 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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14 adverse events reported
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