Buspirone Hydrochloride

Product NDC

70518-0264

11-digit product format

705180264

Labeler code

70518

Product ID

70518-0264_9ff0c116-8b32-01cb-e053-2995a90a7bf4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

buspirone hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076008

Marketing category

ANDA

Marketing start

2017-02-27

Marketing end

0000-00-00

Substance

BUSPIRONE HYDROCHLORIDE

Active strength

5 mg/1

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record