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Sulfacetamide Sodium, Sulfur - 67877-268-17 - (Sulfacetamide Sodium, Sulfur)

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Drug Information of Sulfacetamide Sodium, Sulfur

Product NDC: 67877-268
Proprietary Name: Sulfacetamide Sodium, Sulfur
Non Proprietary Name: Sulfacetamide Sodium, Sulfur
Active Ingredient(s): 100; 50    mg/g; mg/g & nbsp;   Sulfacetamide Sodium, Sulfur
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfacetamide Sodium, Sulfur

Product NDC: 67877-268
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20111108

Package Information of Sulfacetamide Sodium, Sulfur

Package NDC: 67877-268-17
Package Description: 170.1 g in 1 TUBE (67877-268-17)

NDC Information of Sulfacetamide Sodium, Sulfur

NDC Code 67877-268-17
Proprietary Name Sulfacetamide Sodium, Sulfur
Package Description 170.1 g in 1 TUBE (67877-268-17)
Product NDC 67877-268
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfacetamide Sodium, Sulfur
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20111108
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Ascend Laboratories, 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 Sulfacetamide Sodium, Sulfur


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