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Verapamil Hydrochloride - 55154-6982-8 - (VERAPAMIL HYDROCHLORIDE)

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Drug Information of Verapamil Hydrochloride

Product NDC: 55154-6982
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: 55154-6982
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070737
Marketing Category: ANDA
Start Marketing Date: 20110325

Package Information of Verapamil Hydrochloride

Package NDC: 55154-6982-8
Package Description: 1 VIAL in 1 BAG (55154-6982-8) > 4 mL in 1 VIAL

NDC Information of Verapamil Hydrochloride

NDC Code 55154-6982-8
Proprietary Name Verapamil Hydrochloride
Package Description 1 VIAL in 1 BAG (55154-6982-8) > 4 mL in 1 VIAL
Product NDC 55154-6982
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 Cardinal Health
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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