Amlodipine Besylate

Product NDC

69117-0052

11-digit product format

691170052

Labeler code

69117

Product ID

69117-0052_b705b13c-a52d-3f77-e053-2995a90a5165

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

Yiling Pharmaceutical, Inc.

Application

ANDA076692

Marketing category

ANDA

Marketing start

2007-07-23

Marketing end

0000-00-00

Substance

AMLODIPINE BESYLATE

Active strength

5 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record