Nifedipine

Product NDC

51079-400

11-digit product format

510790400

Labeler code

51079

Product ID

51079-400_7d002b16-caa1-5cee-e053-2991aa0ab577

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA090649

Marketing category

ANDA

Marketing start

2010-09-13

Marketing end

2019-05-31

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

0000-00-00

Current FDA listing

Historical FDA.report record