AMLODIPINE BESYLATE

Product NDC

70518-1677

11-digit product format

705181677

Labeler code

70518

Product ID

70518-1677_961d626f-2c6d-7333-e053-2995a90a0434

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

AMLODIPINE BESYLATE

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078552

Marketing category

ANDA

Marketing start

2018-11-16

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