Nifedipine

Product NDC

49884-679

11-digit product format

498840679

Labeler code

49884

Product ID

49884-679_0fffb6c5-dfc5-4d13-bc1f-d4a35f3f66fe

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Par Pharmaceutical, Inc.

Application

ANDA077899

Marketing category

ANDA

Marketing start

2012-05-29

Marketing end

0000-00-00

Substance

NIFEDIPINE

Active strength

90 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record