Verapamil - 55289-607-30 - (Verapamil)

Alphabetical Index


Drug Information of Verapamil

Product NDC: 55289-607
Proprietary Name: Verapamil
Non Proprietary Name: Verapamil
Active Ingredient(s): 180    mg/1 & nbsp;   Verapamil
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil

Product NDC: 55289-607
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090700
Marketing Category: ANDA
Start Marketing Date: 20110805

Package Information of Verapamil

Package NDC: 55289-607-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-607-30)

NDC Information of Verapamil

NDC Code 55289-607-30
Proprietary Name Verapamil
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-607-30)
Product NDC 55289-607
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110805
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil


General Information