Nifedipine

Product NDC

45963-152

11-digit product format

459630152

Labeler code

45963

Product ID

45963-152_aee69bb7-e5b9-483a-b552-2e67cec9bb34

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Actavis Pharma, Inc.

Application

ANDA077899

Marketing category

ANDA

Marketing start

2012-05-25

Marketing end

2020-08-31

Substance

NIFEDIPINE

Active strength

90 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