Amlodipine Besylate

Product NDC

0093-7168

11-digit product format

000937168

Labeler code

0093

Product ID

0093-7168_3f3a3256-1d0a-4611-a2d7-3c5a88b744d1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA076846

Marketing category

ANDA

Marketing start

2007-07-10

Marketing end

2019-10-31

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