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Verapamil Hydrochloride - 24236-361-02 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 24236-361
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: 24236-361
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070994
Marketing Category: ANDA
Start Marketing Date: 20111213

Package Information of Verapamil Hydrochloride

Package NDC: 24236-361-02
Package Description: 30 TABLET in 1 BLISTER PACK (24236-361-02)

NDC Information of Verapamil Hydrochloride

NDC Code 24236-361-02
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (24236-361-02)
Product NDC 24236-361
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111213
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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