nifedipine - 59762-6692-3 - (NIFEDIPINE)

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Drug Information of nifedipine

Product NDC: 59762-6692
Proprietary Name: nifedipine
Non Proprietary Name: NIFEDIPINE
Active Ingredient(s): 90    mg/1 & nbsp;   NIFEDIPINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of nifedipine

Product NDC: 59762-6692
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019684
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20100331

Package Information of nifedipine

Package NDC: 59762-6692-3
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59762-6692-3)

NDC Information of nifedipine

NDC Code 59762-6692-3
Proprietary Name nifedipine
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59762-6692-3)
Product NDC 59762-6692
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NIFEDIPINE
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100331
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name NIFEDIPINE
Strength Number 90
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of nifedipine


General Information