Labetalol Hydrochloride

Product NDC

0615-7688

11-digit product format

006157688

Labeler code

0615

Product ID

0615-7688_130580ab-9628-452b-b05f-2bd1781b2097

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Labetalol Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA074787

Marketing category

ANDA

Marketing start

2011-01-01

Marketing end

0000-00-00

Substance

LABETALOL HYDROCHLORIDE

Active strength

300 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record