Sumaxin - 43538-100-60 - (sulfacetamide sodium and Sulfur)

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Drug Information of Sumaxin

Product NDC: 43538-100
Proprietary Name: Sumaxin
Non Proprietary Name: sulfacetamide sodium and Sulfur
Active Ingredient(s): 100; 40    mg/g; mg/g & nbsp;   sulfacetamide sodium and Sulfur
Administration Route(s): TOPICAL
Dosage Form(s): CLOTH
Coding System: National Drug Codes(NDC)

Labeler Information of Sumaxin

Product NDC: 43538-100
Labeler Name: Medimetriks Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20090101

Package Information of Sumaxin

Package NDC: 43538-100-60
Package Description: 60 PACKET in 1 CARTON (43538-100-60) > 3.7 g in 1 PACKET

NDC Information of Sumaxin

NDC Code 43538-100-60
Proprietary Name Sumaxin
Package Description 60 PACKET in 1 CARTON (43538-100-60) > 3.7 g in 1 PACKET
Product NDC 43538-100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sulfacetamide sodium and Sulfur
Dosage Form Name CLOTH
Route Name TOPICAL
Start Marketing Date 20090101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Medimetriks Pharmaceuticals, Inc.
Substance Name SULFACETAMIDE SODIUM; SULFUR
Strength Number 100; 40
Strength Unit mg/g; mg/g
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of Sumaxin


General Information