Nifedipine

Product NDC

70518-0792

11-digit product format

705180792

Labeler code

70518

Product ID

70518-0792_8ec93da5-1c7f-1282-e053-2a95a90a7589

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077127

Marketing category

ANDA

Marketing start

2017-10-17

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