Amlodipine Besylate

Product NDC

70518-1597

11-digit product format

705181597

Labeler code

70518

Product ID

70518-1597_9487ede4-8973-3ae1-e053-2995a90aa461

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078043

Marketing category

ANDA

Marketing start

2018-10-26

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

2020-12-31

Current FDA listing

Historical FDA.report record