NDC 71335-1673 – Buspirone Hydrochloride

Buspirone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1673

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210907
Marketed since
November 14, 2019
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-1673-130 TABLET in 1 BOTTLE (71335-1673-1)Jul 28, 2020
71335-1673-260 TABLET in 1 BOTTLE (71335-1673-2)Oct 13, 2020
71335-1673-390 TABLET in 1 BOTTLE (71335-1673-3)Oct 26, 2021
71335-1673-445 TABLET in 1 BOTTLE (71335-1673-4)Apr 4, 2024
71335-1673-5180 TABLET in 1 BOTTLE (71335-1673-5)Jul 24, 2020
71335-1673-6120 TABLET in 1 BOTTLE (71335-1673-6)Dec 22, 2020
71335-1673-710 TABLET in 1 BOTTLE (71335-1673-7)Dec 22, 2020

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