Amlodipine Besylate

Product NDC

70518-0812

11-digit product format

705180812

Labeler code

70518

Product ID

70518-0812_67d756f0-9f86-1638-e053-2991aa0a85c4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

amlodipine besylate

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078414

Marketing category

ANDA

Marketing start

2018-03-20

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