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acid reducer - 11822-0141-4 - (Famotidine)

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Drug Information of acid reducer

Product NDC: 11822-0141
Proprietary Name: acid reducer
Non Proprietary Name: Famotidine
Active Ingredient(s): 10    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of acid reducer

Product NDC: 11822-0141
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075400
Marketing Category: ANDA
Start Marketing Date: 20090910

Package Information of acid reducer

Package NDC: 11822-0141-4
Package Description: 4 BLISTER PACK in 1 CARTON (11822-0141-4) > 10 TABLET in 1 BLISTER PACK

NDC Information of acid reducer

NDC Code 11822-0141-4
Proprietary Name acid reducer
Package Description 4 BLISTER PACK in 1 CARTON (11822-0141-4) > 10 TABLET in 1 BLISTER PACK
Product NDC 11822-0141
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090910
Marketing Category Name ANDA
Labeler Name Rite Aid Corporation
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of acid reducer


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