Labetalol Hydrochloride

Product NDC

70518-0027

11-digit product format

705180027

Labeler code

70518

Product ID

70518-0027_81a698f8-2a1b-6ea1-e053-2991aa0a0ed9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

labetalol hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018716

Marketing category

NDA

Marketing start

2016-11-30

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