Amlodipine Besylate

Product NDC

51655-053

11-digit product format

516550053

Labeler code

51655

Product ID

51655-053_71eaa8fe-12db-4b68-b8a1-7dd54a323b48

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amolodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

Northwind Pharmaceuticals, LLC

Application

ANDA077955

Marketing category

ANDA

Marketing start

2014-09-21

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