Labetalol Hydrochloride

Product NDC

68071-3180

11-digit product format

680713180

Labeler code

68071

Product ID

68071-3180_4b6b2ce1-e2b6-3921-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

labetalol hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

NDA018716

Marketing category

NDA

Marketing start

2014-12-01

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