Nifedipine

Product NDC

50268-600

11-digit product format

502680600

Labeler code

50268

Product ID

50268-600_6c41f385-00aa-4d27-e053-2a91aa0a4195

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

AvPAK

Application

ANDA072579

Marketing category

ANDA

Marketing start

2015-07-29

Marketing end

0000-00-00

Substance

NIFEDIPINE

Active strength

10 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