Amlodipine Besylate

Product NDC

55154-3392

11-digit product format

551543392

Labeler code

55154

Product ID

55154-3392_cf9eb373-4467-4384-a2bb-aa92b8c2608c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

Cardinal Health

Application

ANDA078500

Marketing category

ANDA

Marketing start

2009-06-10

Marketing end

0000-00-00

Substance

AMLODIPINE BESYLATE

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