Buspirone Hydrochloride

Product NDC

70518-0922

11-digit product format

705180922

Labeler code

70518

Product ID

70518-0922_8f58e80d-cd6e-c9b4-e053-2a95a90a00fc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Buspirone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA202330

Marketing category

ANDA

Marketing start

2017-12-26

Marketing end

0000-00-00

Substance

BUSPIRONE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record