Buspirone Hydrochloride

Product NDC

70518-1687

11-digit product format

705181687

Labeler code

70518

Product ID

70518-1687_962ad263-b7cf-3a2e-e053-2995a90a3567

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Buspirone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075022

Marketing category

ANDA

Marketing start

2018-11-21

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