Amlodipine Besylate

Product NDC

63629-6362

11-digit product format

636296362

Labeler code

63629

Product ID

63629-6362_d907826a-2478-4082-bbf1-720d4a1f708c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077262

Marketing category

ANDA

Marketing start

2007-07-09

Marketing end

0000-00-00

Substance

AMLODIPINE BESYLATE

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

2019-12-31

Current FDA listing

Historical FDA.report record