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SODIUM SULFACETAMIDE - 42792-106-12 - (SULFACETAMIDE SODIUM)

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Drug Information of SODIUM SULFACETAMIDE

Product NDC: 42792-106
Proprietary Name: SODIUM SULFACETAMIDE
Non Proprietary Name: SULFACETAMIDE SODIUM
Active Ingredient(s): 100    mg/mL & nbsp;   SULFACETAMIDE SODIUM
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of SODIUM SULFACETAMIDE

Product NDC: 42792-106
Labeler Name: Austin Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110915

Package Information of SODIUM SULFACETAMIDE

Package NDC: 42792-106-12
Package Description: 355 mL in 1 BOTTLE, PLASTIC (42792-106-12)

NDC Information of SODIUM SULFACETAMIDE

NDC Code 42792-106-12
Proprietary Name SODIUM SULFACETAMIDE
Package Description 355 mL in 1 BOTTLE, PLASTIC (42792-106-12)
Product NDC 42792-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SULFACETAMIDE SODIUM
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110915
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Austin Pharmaceuticals, LLC
Substance Name SULFACETAMIDE SODIUM
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of SODIUM SULFACETAMIDE


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