Nifedipine

Product NDC

50090-3035

11-digit product format

500903035

Labeler code

50090

Product ID

50090-3035_63e3bbc0-c1e4-4c5d-b806-5a10b5a816f7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA077899

Marketing category

ANDA

Marketing start

2016-03-02

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record