Home > National Drug Code (NDC) > Verapamil Hydrochloride

Verapamil Hydrochloride - 0615-7618-39 - (Verapamil Hydrochloride)

Alphabetical Index


Drug Information of Verapamil Hydrochloride

Product NDC: 0615-7618
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: 0615-7618
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070995
Marketing Category: ANDA
Start Marketing Date: 19861001

Package Information of Verapamil Hydrochloride

Package NDC: 0615-7618-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7618-39)

NDC Information of Verapamil Hydrochloride

NDC Code 0615-7618-39
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7618-39)
Product NDC 0615-7618
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 NCS HealthCare of KY, Inc dba Vangard Labs
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


General Information