Amlodipine Besylate

Product NDC

55154-5097

11-digit product format

551545097

Labeler code

55154

Product ID

55154-5097_a3e72e20-95a7-4c81-8cc7-535c01b70e1f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

Cardinal Health

Application

ANDA076418

Marketing category

ANDA

Marketing start

2010-01-14

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record