NDC 71335-0222 – Buspirone hydrochloride

Buspirone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0222

Product details

Brand name
Buspirone hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078888
Marketed since
May 3, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Buspirone hydrochloride →

Package NDC codes (6)

Package NDCDescriptionSince
71335-0222-130 TABLET in 1 BOTTLE (71335-0222-1)Dec 27, 2021
71335-0222-260 TABLET in 1 BOTTLE (71335-0222-2)Apr 11, 2019
71335-0222-390 TABLET in 1 BOTTLE (71335-0222-3)Dec 27, 2021
71335-0222-445 TABLET in 1 BOTTLE (71335-0222-4)Dec 27, 2021
71335-0222-5180 TABLET in 1 BOTTLE (71335-0222-5)Dec 27, 2021
71335-0222-6120 TABLET in 1 BOTTLE (71335-0222-6)Dec 27, 2021

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