Amlodipine Besylate

Product NDC

0179-0213

11-digit product format

001790213

Labeler code

0179

Product ID

0179-0213_7b969549-52e8-5e70-e053-2991aa0a7635

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

ANDA203245

Marketing category

ANDA

Marketing start

2016-07-08

Marketing end

2020-08-31

Substance

AMLODIPINE BESYLATE

Active strength

10 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