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Acid Reducer - 41250-194-02 - (Famotidine)

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Drug Information of Acid Reducer

Product NDC: 41250-194
Proprietary Name: 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 Acid Reducer

Product NDC: 41250-194
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077351
Marketing Category: ANDA
Start Marketing Date: 20060929

Package Information of Acid Reducer

Package NDC: 41250-194-02
Package Description: 5 BLISTER PACK in 1 CARTON (41250-194-02) > 5 TABLET in 1 BLISTER PACK

NDC Information of Acid Reducer

NDC Code 41250-194-02
Proprietary Name Acid Reducer
Package Description 5 BLISTER PACK in 1 CARTON (41250-194-02) > 5 TABLET in 1 BLISTER PACK
Product NDC 41250-194
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060929
Marketing Category Name ANDA
Labeler Name Meijer Distribution Inc
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acid Reducer


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