Buspirone Hydrochloride

Product NDC

70518-0203

11-digit product format

705180203

Labeler code

70518

Product ID

70518-0203_9f895502-5b19-6bd2-e053-2a95a90acdcb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

buspirone hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076008

Marketing category

ANDA

Marketing start

2017-02-07

Marketing end

0000-00-00

Substance

BUSPIRONE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record