AMLODIPINE BESYLATE

Product NDC

50268-083

11-digit product format

502680083

Labeler code

50268

Product ID

50268-083_76157ba1-4556-d942-e053-2991aa0ad985

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

AMLODIPINE BESYLATE

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA078552

Marketing category

ANDA

Marketing start

2014-01-23

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