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SODIUM SULFACETAMIDE - 42192-129-16 - (SODIUM SULFACETAMIDE)

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Drug Information of SODIUM SULFACETAMIDE

Product NDC: 42192-129
Proprietary Name: SODIUM SULFACETAMIDE
Non Proprietary Name: SODIUM SULFACETAMIDE
Active Ingredient(s): 100    mg/mL & nbsp;   SODIUM SULFACETAMIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of SODIUM SULFACETAMIDE

Product NDC: 42192-129
Labeler Name: Acella Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20101214

Package Information of SODIUM SULFACETAMIDE

Package NDC: 42192-129-16
Package Description: 480 mL in 1 BOTTLE (42192-129-16)

NDC Information of SODIUM SULFACETAMIDE

NDC Code 42192-129-16
Proprietary Name SODIUM SULFACETAMIDE
Package Description 480 mL in 1 BOTTLE (42192-129-16)
Product NDC 42192-129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM SULFACETAMIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20101214
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Acella 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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