Sotalol Hydrochloride

Product NDC

0603-5770

11-digit product format

006035770

Labeler code

0603

Product ID

0603-5770_2398995d-e533-4306-a436-eb87ff0f064f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sotalol Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical

Application

ANDA075563

Marketing category

ANDA

Marketing start

2003-11-07

Marketing end

2019-03-31

Substance

SOTALOL HYDROCH

Active strength

120 mg/1

Pharmacologic classes

Antiarrhythmic

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record