Buspirone Hydrochloride

Product NDC

70518-1820

11-digit product format

705181820

Labeler code

70518

Product ID

70518-1820_840333e5-0697-3d23-e053-2a91aa0a79f5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

buspirone hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076008

Marketing category

ANDA

Marketing start

2019-01-24

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