Buspirone Hydrochloride

Product NDC

70518-0737

11-digit product format

705180737

Labeler code

70518

Product ID

70518-0737_8c5977b1-58a2-30de-e053-2995a90accd4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Buspirone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA202557

Marketing category

ANDA

Marketing start

2017-09-18

Marketing end

0000-00-00

Substance

BUSPIRONE HYDROCHLORIDE

Active strength

15 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record