Amlodipine Besylate

Product NDC

60687-477

11-digit product format

606870477

Labeler code

60687

Product ID

60687-477_8d812959-044f-6617-e053-2a95a90a8df3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine besylate

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA078925

Marketing category

ANDA

Marketing start

2019-07-15

Marketing end

0000-00-00

Substance

AMLODIPINE BESYLATE

Active strength

3 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