amlodipine besylate

Product NDC

59762-1520

11-digit product format

597621520

Labeler code

59762

Product ID

59762-1520_4b488534-377e-4fbb-93fb-3bd140782d3a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amlodipine besylate

Dosage form

TABLET

Route

ORAL

Labeler

Greenstone LLC

Application

NDA019787

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2007-03-23

Marketing end

2020-03-31

Substance

AMLODIPINE BESYLATE

Active strength

3 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