Sotalol Hydrochloride

Product NDC

63629-4719

11-digit product format

636294719

Labeler code

63629

Product ID

63629-4719_ec395446-2ce2-48aa-ac6b-1368b5f81e04

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sotalol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA075563

Marketing category

ANDA

Marketing start

2003-11-07

Marketing end

0000-00-00

Substance

SOTALOL HYDROCHLORIDE

Active strength

80 mg/1

Pharmacologic classes

Antiarrhythmic [EPC],Cardiac Rhythm Alteration [PE],Adrenergic beta-Antagonists [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record