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Verapamil Hydrochloride - 54868-0121-3 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 54868-0121
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: Verapamil Hydrochloride
Active Ingredient(s): 120    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: 54868-0121
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070994
Marketing Category: ANDA
Start Marketing Date: 19960205

Package Information of Verapamil Hydrochloride

Package NDC: 54868-0121-3
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (54868-0121-3)

NDC Information of Verapamil Hydrochloride

NDC Code 54868-0121-3
Proprietary Name Verapamil Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (54868-0121-3)
Product NDC 54868-0121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19960205
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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