Sumaxin - 43538-130-16 - (sodium sulfacetamide 9%-sulfur 4%)

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Drug Information of Sumaxin

Product NDC: 43538-130
Proprietary Name: Sumaxin
Non Proprietary Name: sodium sulfacetamide 9%-sulfur 4%
Active Ingredient(s): 90; 40    mg/g; mg/g & nbsp;   sodium sulfacetamide 9%-sulfur 4%
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sumaxin

Product NDC: 43538-130
Labeler Name: Medimetriks Pharmaceutical inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED OTHER
Start Marketing Date: 20091030

Package Information of Sumaxin

Package NDC: 43538-130-16
Package Description: 1 BOTTLE in 1 CARTON (43538-130-16) > 453.5 g in 1 BOTTLE

NDC Information of Sumaxin

NDC Code 43538-130-16
Proprietary Name Sumaxin
Package Description 1 BOTTLE in 1 CARTON (43538-130-16) > 453.5 g in 1 BOTTLE
Product NDC 43538-130
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sodium sulfacetamide 9%-sulfur 4%
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20091030
Marketing Category Name UNAPPROVED OTHER
Labeler Name Medimetriks Pharmaceutical inc
Substance Name SULFACETAMIDE SODIUM; SULFUR
Strength Number 90; 40
Strength Unit mg/g; mg/g
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of Sumaxin


General Information