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Verapamil Hydrochloride - 0409-4011-01 - (VERAPAMIL HYDROCHLORIDE)

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Drug Information of Verapamil Hydrochloride

Product NDC: 0409-4011
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: VERAPAMIL HYDROCHLORIDE
Active Ingredient(s): 2.5    mg/mL & nbsp;   VERAPAMIL HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 0409-4011
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070738
Marketing Category: ANDA
Start Marketing Date: 20110325

Package Information of Verapamil Hydrochloride

Package NDC: 0409-4011-01
Package Description: 5 AMPULE in 1 CONTAINER (0409-4011-01) > 2 mL in 1 AMPULE

NDC Information of Verapamil Hydrochloride

NDC Code 0409-4011-01
Proprietary Name Verapamil Hydrochloride
Package Description 5 AMPULE in 1 CONTAINER (0409-4011-01) > 2 mL in 1 AMPULE
Product NDC 0409-4011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VERAPAMIL HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110325
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 2.5
Strength Unit mg/mL
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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