MedPath

SULFACETAMIDE SODIUM

SULFACETAMIDE SODIUM - sulfacetamide sodium solution

Approved
Approval ID

1c490337-c060-4f85-9998-f292edea92eb

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 12, 2010

Manufacturers
FDA

Keltman Pharmaceuticals Inc.

DUNS: 362861077

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

SULFACETAMIDE SODIUM

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code68387-491
Application NumberANDA089560
Product Classification
M
Marketing Category
C73584
G
Generic Name
SULFACETAMIDE SODIUM
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateJuly 12, 2010
FDA Product Classification

INGREDIENTS (6)

SULFACETAMIDE SODIUMActive
Quantity: 100 mg in 1 mL
Code: 4NRT660KJQ
Classification: ACTIB
SODIUM THIOSULFATEInactive
Code: HX1032V43M
Classification: IACT
METHYLCELLULOSE (100 CPS)Inactive
Code: 4GFU244C4J
Classification: IACT
METHYLPARABENInactive
Code: A2I8C7HI9T
Classification: IACT
PROPYLPARABENInactive
Code: Z8IX2SC1OH
Classification: IACT
SODIUM PHOSPHATE, MONOBASICInactive
Code: 3980JIH2SW
Classification: IACT

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

SULFACETAMIDE SODIUM - FDA Drug Approval Details