Amlodipine Besylate

Product NDC

48433-308

11-digit product format

484330308

Labeler code

48433

Product ID

48433-308_790129ef-6a1b-45cb-8b02-25fa8a40c2ba

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amlodipine besylate

Dosage form

TABLET

Route

ORAL

Labeler

Safecor Health, LLC

Application

ANDA078414

Marketing category

ANDA

Marketing start

2014-09-30

Marketing end

0000-00-00

Substance

AMLODIPINE BESYLATE

Active strength

5 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