Nifedipine

Product NDC

10370-677

11-digit product format

103700677

Labeler code

10370

Product ID

10370-677_4d6be233-5b05-4efe-88ff-370ca1be90e4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Par Pharmaceutical, Inc.

Application

ANDA077899

Marketing category

ANDA

Marketing start

2016-03-02

Marketing end

2019-11-30

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