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Verapamil Hydrochloride - 21695-512-90 - (verapamil hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 21695-512
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
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 21695-512
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070856
Marketing Category: ANDA
Start Marketing Date: 19960205

Package Information of Verapamil Hydrochloride

Package NDC: 21695-512-90
Package Description: 90 TABLET in 1 BOTTLE (21695-512-90)

NDC Information of Verapamil Hydrochloride

NDC Code 21695-512-90
Proprietary Name Verapamil Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (21695-512-90)
Product NDC 21695-512
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960205
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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