Amlodipine Besylate

Product NDC

42708-008

11-digit product format

427080008

Labeler code

42708

Product ID

42708-008_28bbb62a-8bca-4779-a632-d55ac7df9987

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

QPharma Inc

Application

ANDA076846

Marketing category

ANDA

Marketing start

2007-07-10

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

2020-12-31

Current FDA listing

Historical FDA.report record