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verapamil hydrochloride - 60760-984-30 - (verapamil hydrochloride)

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Drug Information of verapamil hydrochloride

Product NDC: 60760-984
Proprietary Name: verapamil hydrochloride
Non Proprietary Name: verapamil hydrochloride
Active Ingredient(s): 240    mg/1 & nbsp;   verapamil hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of verapamil hydrochloride

Product NDC: 60760-984
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078906
Marketing Category: ANDA
Start Marketing Date: 20130522

Package Information of verapamil hydrochloride

Package NDC: 60760-984-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-984-30)

NDC Information of verapamil hydrochloride

NDC Code 60760-984-30
Proprietary Name verapamil hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-984-30)
Product NDC 60760-984
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130522
Marketing Category Name ANDA
Labeler Name St Marys Medical Park Pharmacy
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 240
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of verapamil hydrochloride


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