Amlodipine Besylate

Product NDC

68788-9314

11-digit product format

687889314

Labeler code

68788

Product ID

68788-9314_28501a6a-639c-4154-8ebf-f6088231e1e5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA077955

Marketing category

ANDA

Marketing start

2015-04-06

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