Labetalol HCl

Product NDC

60687-125

11-digit product format

606870125

Labeler code

60687

Product ID

60687-125_8647e2c1-e6ee-cc83-e053-2a91aa0aec79

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Labetalol HCl

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA075113

Marketing category

ANDA

Marketing start

2015-10-27

Marketing end

2020-10-31

Substance

LABETALOL HYDROCHLORIDE

Active strength

200 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record