Verelan - 54868-4591-0 - (verapamil hydrochloride)

Alphabetical Index


Drug Information of Verelan

Product NDC: 54868-4591
Proprietary Name: Verelan
Non Proprietary Name: verapamil hydrochloride
Active Ingredient(s): 360    mg/1 & nbsp;   verapamil hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE PELLETS
Coding System: National Drug Codes(NDC)

Labeler Information of Verelan

Product NDC: 54868-4591
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019614
Marketing Category: NDA
Start Marketing Date: 20030612

Package Information of Verelan

Package NDC: 54868-4591-0
Package Description: 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (54868-4591-0)

NDC Information of Verelan

NDC Code 54868-4591-0
Proprietary Name Verelan
Package Description 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (54868-4591-0)
Product NDC 54868-4591
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name CAPSULE, DELAYED RELEASE PELLETS
Route Name ORAL
Start Marketing Date 20030612
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 360
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verelan


General Information