AMLODIPINE BESYLATE

Product NDC

48792-7840

11-digit product format

487927840

Labeler code

48792

Product ID

48792-7840_6ba99be0-6ab3-f139-e053-2991aa0a6401

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

AMLODIPINE BESYLATE

Dosage form

TABLET

Route

ORAL

Labeler

Sunshine Lake Pharma Co., Ltd.

Application

ANDA206524

Marketing category

ANDA

Marketing start

2018-05-07

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