Labetalol hydrochloride

Product NDC

60429-278

11-digit product format

604290278

Labeler code

60429

Product ID

60429-278_7a07f7b3-78aa-0d61-e053-2a91aa0aa0e3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Labetalol hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Golden State Medical Supply, Inc.

Application

ANDA075133

Marketing category

ANDA

Marketing start

2013-04-16

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

2020-12-31

Current FDA listing

Historical FDA.report record