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Verapamil Hydrochloride - 55289-481-30 - (verapamil hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 55289-481
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: verapamil hydrochloride
Active Ingredient(s): 120    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: 55289-481
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071483
Marketing Category: ANDA
Start Marketing Date: 20110504

Package Information of Verapamil Hydrochloride

Package NDC: 55289-481-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-481-30)

NDC Information of Verapamil Hydrochloride

NDC Code 55289-481-30
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-481-30)
Product NDC 55289-481
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110504
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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