Nifedipine

Product NDC

49999-357

11-digit product format

499990357

Labeler code

49999

Product ID

49999-357_f4ed3236-3a27-457d-88dd-3820b81d4fac

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA077127

Marketing category

ANDA

Marketing start

2005-11-21

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

2019-12-31

Current FDA listing

Historical FDA.report record