Amlodipine Besylate

Product NDC

0603-2108

11-digit product format

006032108

Labeler code

0603

Product ID

0603-2108_b4e48976-a292-4faa-a07a-9f86269b208d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amlodipine besylate

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical

Application

ANDA078414

Marketing category

ANDA

Marketing start

2010-04-07

Marketing end

2019-04-30

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