Amlodipine Besylate

Product NDC

68788-1737

11-digit product format

687881737

Labeler code

68788

Product ID

68788-1737_558333c8-9d13-4dc2-8f8b-d51cded3ec49

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amlodipine besylate

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA078414

Marketing category

ANDA

Marketing start

2010-04-07

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