Nifedipine

Product NDC

70518-0747

11-digit product format

705180747

Labeler code

70518

Product ID

70518-0747_8e7b7cb1-e981-5489-e053-2995a90ae742

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA201071

Marketing category

ANDA

Marketing start

2017-09-25

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record