nifedipine

Product NDC

59762-6690

11-digit product format

597626690

Labeler code

59762

Product ID

59762-6690_d6a5443f-c368-4b51-917f-fba3fc92ef58

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Greenstone LLC

Application

NDA019684

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2010-03-31

Marketing end

0000-00-00

Substance

NIFEDIPINE

Active strength

30 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record