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Sunmark Acid Reducer - 49348-442-13 - (Famotidine)

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Drug Information of Sunmark Acid Reducer

Product NDC: 49348-442
Proprietary Name: Sunmark Acid Reducer
Non Proprietary Name: Famotidine
Active Ingredient(s): 10    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark Acid Reducer

Product NDC: 49348-442
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075312
Marketing Category: ANDA
Start Marketing Date: 20030811

Package Information of Sunmark Acid Reducer

Package NDC: 49348-442-13
Package Description: 1 BOTTLE in 1 CARTON (49348-442-13) > 90 TABLET, COATED in 1 BOTTLE

NDC Information of Sunmark Acid Reducer

NDC Code 49348-442-13
Proprietary Name Sunmark Acid Reducer
Package Description 1 BOTTLE in 1 CARTON (49348-442-13) > 90 TABLET, COATED in 1 BOTTLE
Product NDC 49348-442
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20030811
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sunmark Acid Reducer


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