Sotalol Hydrochloride

Product NDC

68071-2014

11-digit product format

680712014

Labeler code

68071

Product ID

68071-2014_46df076d-4e39-6faa-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sotalol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record