Amlodipine Besylate

Product NDC

51079-450

11-digit product format

510790450

Labeler code

51079

Product ID

51079-450_7b2018ec-84d3-6b95-e053-2a91aa0a2626

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amlodipine besylate

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA076418

Marketing category

ANDA

Marketing start

2007-04-02

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