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SunMark Acid Reducer - 49348-817-05 - (Famotidine)

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Drug Information of SunMark Acid Reducer

Product NDC: 49348-817
Proprietary Name: SunMark Acid Reducer
Non Proprietary Name: Famotidine
Active Ingredient(s): 20    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of SunMark Acid Reducer

Product NDC: 49348-817
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077351
Marketing Category: ANDA
Start Marketing Date: 20070618

Package Information of SunMark Acid Reducer

Package NDC: 49348-817-05
Package Description: 5 BLISTER PACK in 1 CARTON (49348-817-05) > 5 TABLET in 1 BLISTER PACK

NDC Information of SunMark Acid Reducer

NDC Code 49348-817-05
Proprietary Name SunMark Acid Reducer
Package Description 5 BLISTER PACK in 1 CARTON (49348-817-05) > 5 TABLET in 1 BLISTER PACK
Product NDC 49348-817
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070618
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of SunMark Acid Reducer


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