Amlodipine Besylate

Product NDC

60687-285

11-digit product format

606870285

Labeler code

60687

Product ID

60687-285_800d5335-b5c1-1c40-e053-2991aa0ab922

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA077955

Marketing category

ANDA

Marketing start

2017-02-06

Marketing end

2019-10-31

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