VERELAN - 0091-2491-23 - (verapamil hydrochloride)

Alphabetical Index


Drug Information of VERELAN

Product NDC: 0091-2491
Proprietary Name: VERELAN
Non Proprietary Name: verapamil hydrochloride
Active Ingredient(s): 240    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: 0091-2491
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019614
Marketing Category: NDA
Start Marketing Date: 19900529

Package Information of VERELAN

Package NDC: 0091-2491-23
Package Description: 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0091-2491-23)

NDC Information of VERELAN

NDC Code 0091-2491-23
Proprietary Name VERELAN
Package Description 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0091-2491-23)
Product NDC 0091-2491
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name CAPSULE, DELAYED RELEASE PELLETS
Route Name ORAL
Start Marketing Date 19900529
Marketing Category Name NDA
Labeler Name UCB, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 240
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of VERELAN


General Information