Buspirone Hydrochloride

Product NDC

68788-5665

11-digit product format

687885665

Labeler code

68788

Product ID

68788-5665_60c171e4-071f-45cb-ab90-be1a8c5e9f2c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Buspirone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA075022

Marketing category

ANDA

Marketing start

2012-03-29

Marketing end

0000-00-00

Substance

BUSPIRONE HYDROCHLORIDE

Active strength

15 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record