sotalol hydrochloride

Product NDC

43063-133

11-digit product format

430630133

Labeler code

43063

Product ID

43063-133_7c482b37-3962-e545-e053-2991aa0a167e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

sotalol hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA075366

Marketing category

ANDA

Marketing start

2000-05-01

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

2019-12-31

Current FDA listing

Historical FDA.report record