Famotidine - 68645-140-59 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 68645-140
Proprietary Name: Famotidine
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 Famotidine

Product NDC: 68645-140
Labeler Name: Legacy Pharmaceutical Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075511
Marketing Category: ANDA
Start Marketing Date: 20091026

Package Information of Famotidine

Package NDC: 68645-140-59
Package Description: 60 TABLET in 1 BOTTLE (68645-140-59)

NDC Information of Famotidine

NDC Code 68645-140-59
Proprietary Name Famotidine
Package Description 60 TABLET in 1 BOTTLE (68645-140-59)
Product NDC 68645-140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091026
Marketing Category Name ANDA
Labeler Name Legacy Pharmaceutical Packaging
Substance Name FAMOTIDINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Famotidine


General Information