Nifedipine

Product NDC

50436-4069

11-digit product format

504364069

Labeler code

50436

Product ID

50436-4069_3f490c79-a773-46be-ae11-6ecbcac231ae

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA077127

Marketing category

ANDA

Marketing start

2005-11-21

Marketing end

0000-00-00

Substance

NIFEDIPINE

Active strength

60 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record