Nifedipine

Product NDC

60687-269

11-digit product format

606870269

Labeler code

60687

Product ID

60687-269_7df3b8ab-7634-13f2-e053-2a91aa0a5afc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

American Health Packaging

Application

ANDA077899

Marketing category

ANDA

Marketing start

2016-12-06

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