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Acid Controller - 0363-0701-02 - (Famotidine)

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Drug Information of Acid Controller

Product NDC: 0363-0701
Proprietary Name: Acid Controller
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 Controller

Product NDC: 0363-0701
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077351
Marketing Category: ANDA
Start Marketing Date: 20060926

Package Information of Acid Controller

Package NDC: 0363-0701-02
Package Description: 5 BLISTER PACK in 1 CARTON (0363-0701-02) > 5 TABLET in 1 BLISTER PACK

NDC Information of Acid Controller

NDC Code 0363-0701-02
Proprietary Name Acid Controller
Package Description 5 BLISTER PACK in 1 CARTON (0363-0701-02) > 5 TABLET in 1 BLISTER PACK
Product NDC 0363-0701
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060926
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acid Controller


General Information