VERELAN PM - 0091-4087-01 - (verapamil hydrochloride)

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Drug Information of VERELAN PM

Product NDC: 0091-4087
Proprietary Name: VERELAN PM
Non Proprietary Name: verapamil hydrochloride
Active Ingredient(s): 300    mg/1 & nbsp;   verapamil hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of VERELAN PM

Product NDC: 0091-4087
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020943
Marketing Category: NDA
Start Marketing Date: 19981125

Package Information of VERELAN PM

Package NDC: 0091-4087-01
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0091-4087-01)

NDC Information of VERELAN PM

NDC Code 0091-4087-01
Proprietary Name VERELAN PM
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0091-4087-01)
Product NDC 0091-4087
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19981125
Marketing Category Name NDA
Labeler Name UCB, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of VERELAN PM


General Information