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Verapamil Hydrochloride - 23155-026-05 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 23155-026
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
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 23155-026
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071880
Marketing Category: ANDA
Start Marketing Date: 20110107

Package Information of Verapamil Hydrochloride

Package NDC: 23155-026-05
Package Description: 500 TABLET in 1 BOTTLE (23155-026-05)

NDC Information of Verapamil Hydrochloride

NDC Code 23155-026-05
Proprietary Name Verapamil Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (23155-026-05)
Product NDC 23155-026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110107
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
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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