AMLODIPINE BESYLATE

Product NDC

55700-740

11-digit product format

557000740

Labeler code

55700

Product ID

55700-740_257b7523-1f66-4a34-ba4a-e79bc7b0b5db

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

AMLODIPINE BESYLATE

Dosage form

TABLET

Route

ORAL

Labeler

Quality Care Products, LLC

Application

ANDA077516

Marketing category

ANDA

Marketing start

2019-04-05

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

2020-12-31

Current FDA listing

Historical FDA.report record