Amlodipine Besylate

Product NDC

60760-239

11-digit product format

607600239

Labeler code

60760

Product ID

60760-239_78fe8c84-4579-9919-e053-2a91aa0a97d8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

St Marys Medical Park Pharmacy

Application

ANDA077955

Marketing category

ANDA

Marketing start

2011-09-01

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record