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Sodium Sulfacetamide, Sulfur - 42808-111-45 - (Sodium Sulfacetamide, Sulfur)

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Drug Information of Sodium Sulfacetamide, Sulfur

Product NDC: 42808-111
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): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Sulfacetamide, Sulfur

Product NDC: 42808-111
Labeler Name: Exact-Rx, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110801

Package Information of Sodium Sulfacetamide, Sulfur

Package NDC: 42808-111-45
Package Description: 1 TUBE in 1 CARTON (42808-111-45) > 45 g in 1 TUBE

NDC Information of Sodium Sulfacetamide, Sulfur

NDC Code 42808-111-45
Proprietary Name Sodium Sulfacetamide, Sulfur
Package Description 1 TUBE in 1 CARTON (42808-111-45) > 45 g in 1 TUBE
Product NDC 42808-111
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Sulfacetamide, Sulfur
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20110801
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Exact-Rx, Inc.
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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