NDC 71335-2081 – Buspirone Hydrochloride

Buspirone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2081

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078246
Marketed since
February 21, 2020
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-2081-130 TABLET in 1 BOTTLE (71335-2081-1)May 2, 2022
71335-2081-260 TABLET in 1 BOTTLE (71335-2081-2)May 2, 2022
71335-2081-390 TABLET in 1 BOTTLE (71335-2081-3)May 2, 2022
71335-2081-445 TABLET in 1 BOTTLE (71335-2081-4)May 2, 2022
71335-2081-5180 TABLET in 1 BOTTLE (71335-2081-5)May 2, 2022
71335-2081-6120 TABLET in 1 BOTTLE (71335-2081-6)May 2, 2022

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