Nifedipine

Product NDC

55154-5368

11-digit product format

551545368

Labeler code

55154

Product ID

55154-5368_79046dde-2a61-4a15-8ebb-1dfee4123507

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Cardinal Health

Application

ANDA090649

Marketing category

ANDA

Marketing start

2010-06-23

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

2020-12-31

Current FDA listing

Historical FDA.report record