Labetalol Hydrochloride

Product NDC

70518-1887

11-digit product format

705181887

Labeler code

70518

Product ID

70518-1887_96a60ad6-3738-c358-e053-2a95a90a2fdf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

labetalol hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018716

Marketing category

NDA

Marketing start

2019-02-20

Marketing end

0000-00-00

Substance

LABETALOL HYDROCHLORIDE

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record