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Nisoldipine - 54868-5931-0 - (Nisoldipine)

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Drug Information of Nisoldipine

Product NDC: 54868-5931
Proprietary Name: Nisoldipine
Non Proprietary Name: Nisoldipine
Active Ingredient(s): 40    mg/1 & nbsp;   Nisoldipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Nisoldipine

Product NDC: 54868-5931
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079051
Marketing Category: ANDA
Start Marketing Date: 20080829

Package Information of Nisoldipine

Package NDC: 54868-5931-0
Package Description: 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5931-0)

NDC Information of Nisoldipine

NDC Code 54868-5931-0
Proprietary Name Nisoldipine
Package Description 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5931-0)
Product NDC 54868-5931
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nisoldipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080829
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name NISOLDIPINE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Calcium Channel Antagonists [MoA],Decreased Blood Pressure [PE]

Complete Information of Nisoldipine


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