Felodipine

Product NDC

0378-5013

11-digit product format

003785013

Labeler code

0378

Product ID

0378-5013_2727fa5d-7ba0-4fd4-a1f3-cd6a7108e5bc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Felodipine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA078855

Marketing category

ANDA

Marketing start

2008-04-18

Marketing end

2019-10-31

Substance

FELODIPINE

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

0000-00-00

Current FDA listing

Historical FDA.report record