Buspirone Hydrochloride

Approved

Approval ID

eb072818-3ca8-430b-91a1-e7fedd37990c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 29, 2023

Manufacturers

FDA

Bryant Ranch Prepack

DUNS: 171714327

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code72162-1927

Application NumberANDA078302

Marketing CategoryC73584

Route of AdministrationORAL

Effective DateAugust 29, 2023

Generic Namebuspirone hydrochloride

BUSPIRONE HYDROCHLORIDEActive

Quantity: 30 mg in 1 1

Code: 207LT9J9OC

Classification: ACTIB

SILICON DIOXIDEInactive

Code: ETJ7Z6XBU4

Classification: IACT

ANHYDROUS LACTOSEInactive

Code: 3SY5LH9PMK

Classification: IACT

MICROCRYSTALLINE CELLULOSE 102Inactive

Code: PNR0YF693Y

Classification: IACT

MAGNESIUM STEARATEInactive

Code: 70097M6I30

Classification: IACT

SODIUM STARCH GLYCOLATE TYPE A POTATOInactive

Code: 5856J3G2A2

Classification: IACT