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Verapamil Hydrochloride - 55154-0695-0 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 55154-0695
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: Verapamil Hydrochloride
Active Ingredient(s): 80    mg/1 & nbsp;   Verapamil Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 55154-0695
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070995
Marketing Category: ANDA
Start Marketing Date: 19861001

Package Information of Verapamil Hydrochloride

Package NDC: 55154-0695-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0695-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Verapamil Hydrochloride

NDC Code 55154-0695-0
Proprietary Name Verapamil Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-0695-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-0695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19861001
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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