Buspirone Hydrochloride

Product NDC

70518-0641

11-digit product format

705180641

Labeler code

70518

Product ID

70518-0641_7fade267-f1a0-5741-e053-2991aa0a83fc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

buspirone hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076008

Marketing category

ANDA

Marketing start

2017-07-28

Marketing end

0000-00-00

Substance

BUSPIRONE HYDROCHLORIDE

Active strength

30 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record