Nifedipine

Product NDC

0615-6563

11-digit product format

006156563

Labeler code

0615

Product ID

0615-6563_a90a7ddb-457e-4ab4-b63e-c9f3b186f26a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA090649

Marketing category

ANDA

Marketing start

2010-06-30

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record