Felodipine

Product NDC

51079-467

11-digit product format

510790467

Labeler code

51079

Product ID

51079-467_7be980eb-7389-fd21-e053-2a91aa0af1d5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Felodipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA078855

Marketing category

ANDA

Marketing start

2008-05-01

Marketing end

2019-06-30

Substance

FELODIPINE

Active strength

5 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