NDC 71335-1924 – Buspirone Hydrochloride

Buspirone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1924

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 (6)

Package NDCDescriptionSince
71335-1924-190 TABLET in 1 BOTTLE, PLASTIC (71335-1924-1)Aug 12, 2021
71335-1924-245 TABLET in 1 BOTTLE, PLASTIC (71335-1924-2)Oct 19, 2022
71335-1924-330 TABLET in 1 BOTTLE, PLASTIC (71335-1924-3)Dec 13, 2021
71335-1924-460 TABLET in 1 BOTTLE, PLASTIC (71335-1924-4)Nov 29, 2021
71335-1924-5180 TABLET in 1 BOTTLE, PLASTIC (71335-1924-5)Apr 5, 2024
71335-1924-6120 TABLET in 1 BOTTLE, PLASTIC (71335-1924-6)Apr 5, 2024

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