Labetalol Hydrochloride

Product NDC

50090-2428

11-digit product format

500902428

Labeler code

50090

Product ID

50090-2428_21da522d-6b33-4fa8-9376-b28d244c9f52

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

labetalol hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

NDA018716

Marketing category

NDA

Marketing start

2014-12-01

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record