Famotidine - 0069-0121-02 - (FAMOTIDINE)

Alphabetical Index


Drug Information of Famotidine

Product NDC: 0069-0121
Proprietary Name: Famotidine
Non Proprietary Name: FAMOTIDINE
Active Ingredient(s): 10    mg/mL & nbsp;   FAMOTIDINE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Famotidine

Product NDC: 0069-0121
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078642
Marketing Category: ANDA
Start Marketing Date: 20110510

Package Information of Famotidine

Package NDC: 0069-0121-02
Package Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (0069-0121-02) > 2 mL in 1 VIAL, SINGLE-DOSE (0069-0121-01)

NDC Information of Famotidine

NDC Code 0069-0121-02
Proprietary Name Famotidine
Package Description 25 VIAL, SINGLE-DOSE in 1 CARTON (0069-0121-02) > 2 mL in 1 VIAL, SINGLE-DOSE (0069-0121-01)
Product NDC 0069-0121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FAMOTIDINE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110510
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Famotidine


General Information