Nifedipine

Product NDC

68071-3382

11-digit product format

680713382

Labeler code

68071

Product ID

68071-3382_53fbc93a-7863-33c1-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA076070

Marketing category

ANDA

Marketing start

2002-08-16

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record