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SODIUM SULFACETAMIDE, SULFUR - 42792-107-01 - (SODIUM SULFACETAMIDE, SULFUR)

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Drug Information of SODIUM SULFACETAMIDE, SULFUR

Product NDC: 42792-107
Proprietary Name: SODIUM SULFACETAMIDE, SULFUR
Non Proprietary Name: SODIUM SULFACETAMIDE, SULFUR
Active Ingredient(s): 100; 50    mg/g; mg/g & nbsp;   SODIUM SULFACETAMIDE, SULFUR
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of SODIUM SULFACETAMIDE, SULFUR

Product NDC: 42792-107
Labeler Name: AUSTIN PHARMACEUTICALS, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110604

Package Information of SODIUM SULFACETAMIDE, SULFUR

Package NDC: 42792-107-01
Package Description: 30 g in 1 BOTTLE (42792-107-01)

NDC Information of SODIUM SULFACETAMIDE, SULFUR

NDC Code 42792-107-01
Proprietary Name SODIUM SULFACETAMIDE, SULFUR
Package Description 30 g in 1 BOTTLE (42792-107-01)
Product NDC 42792-107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM SULFACETAMIDE, SULFUR
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110604
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name AUSTIN PHARMACEUTICALS, LLC
Substance Name SULFACETAMIDE SODIUM; SULFUR
Strength Number 100; 50
Strength Unit mg/g; mg/g
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of SODIUM SULFACETAMIDE, SULFUR


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