Klaron - 54868-5401-0 - (sulfacetamide sodium)

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Drug Information of Klaron

Product NDC: 54868-5401
Proprietary Name: Klaron
Non Proprietary Name: sulfacetamide sodium
Active Ingredient(s): 10    mg/mL & nbsp;   sulfacetamide sodium
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Klaron

Product NDC: 54868-5401
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019931
Marketing Category: NDA
Start Marketing Date: 20050901

Package Information of Klaron

Package NDC: 54868-5401-0
Package Description: 118 mL in 1 BOTTLE, PLASTIC (54868-5401-0)

NDC Information of Klaron

NDC Code 54868-5401-0
Proprietary Name Klaron
Package Description 118 mL in 1 BOTTLE, PLASTIC (54868-5401-0)
Product NDC 54868-5401
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sulfacetamide sodium
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20050901
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name SULFACETAMIDE SODIUM
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of Klaron


General Information