Famotidine - 0641-6021-10 - (Famotidine)

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Drug Information of Famotidine

Product NDC: 0641-6021
Proprietary Name: Famotidine
Non Proprietary Name: Famotidine
Active Ingredient(s): 10    mg/mL & nbsp;   Famotidine
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Famotidine

Product NDC: 0641-6021
Labeler Name: West-ward Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075488
Marketing Category: ANDA
Start Marketing Date: 20010416

Package Information of Famotidine

Package NDC: 0641-6021-10
Package Description: 10 VIAL in 1 CARTON (0641-6021-10) > 20 mL in 1 VIAL (0641-6021-01)

NDC Information of Famotidine

NDC Code 0641-6021-10
Proprietary Name Famotidine
Package Description 10 VIAL in 1 CARTON (0641-6021-10) > 20 mL in 1 VIAL (0641-6021-01)
Product NDC 0641-6021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famotidine
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20010416
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp.
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