Amlodipine Besylate

Product NDC

51655-054

11-digit product format

516550054

Labeler code

51655

Product ID

51655-054_da8046b5-5bab-4c31-b660-7eb19c19688e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

Northwind Pharmaceuticals, LLC

Application

ANDA077955

Marketing category

ANDA

Marketing start

2014-09-23

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