Nifedipine

Product NDC

68788-9886

11-digit product format

687889886

Labeler code

68788

Product ID

68788-9886_fbf04757-8389-4273-b946-c4a1784bcdea

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA090649

Marketing category

ANDA

Marketing start

2015-04-23

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record