Famotidine - 43386-500-11 - (Famotidine)

Alphabetical Index


Drug Information of Famotidine

Product NDC: 43386-500
Proprietary Name: Famotidine
Non Proprietary Name: Famotidine
Active Ingredient(s): 40    mg/5mL & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Famotidine

Product NDC: 43386-500
Labeler Name: GAVIS Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201695
Marketing Category: ANDA
Start Marketing Date: 20121217

Package Information of Famotidine

Package NDC: 43386-500-11
Package Description: 50 mL in 1 BOTTLE (43386-500-11)

NDC Information of Famotidine

NDC Code 43386-500-11
Proprietary Name Famotidine
Package Description 50 mL in 1 BOTTLE (43386-500-11)
Product NDC 43386-500
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famotidine
Dosage Form Name FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20121217
Marketing Category Name ANDA
Labeler Name GAVIS Pharmaceuticals, LLC
Substance Name FAMOTIDINE
Strength Number 40
Strength Unit mg/5mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Famotidine


General Information