Nifedipine

Product NDC

68084-923

11-digit product format

680840923

Labeler code

68084

Product ID

68084-923_7df2a9a5-205c-30aa-e053-2a91aa0aeeaa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nifedipine

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA072556

Marketing category

ANDA

Marketing start

2015-11-03

Marketing end

2019-07-31

Substance

NIFEDIPINE

Active strength

20 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record