Amlodipine besylate

Product NDC

59115-058

11-digit product format

591150058

Labeler code

59115

Product ID

59115-058_1e1780ca-5513-49a7-9ee3-f27be5b2ccce

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine besylate

Dosage form

TABLET

Route

ORAL

Labeler

Hikma Pharmaceutical

Application

ANDA077771

Marketing category

ANDA

Marketing start

2011-04-12

Marketing end

0000-00-00

Substance

AMLODIPINE BESYLATE

Active strength

10 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record