NDC 71335-1938 – Buspirone Hydrochloride

Buspirone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1938

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075388
Marketed since
July 27, 2020
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-1938-190 TABLET in 1 BOTTLE (71335-1938-1)Oct 27, 2021
71335-1938-245 TABLET in 1 BOTTLE (71335-1938-2)Apr 8, 2024
71335-1938-330 TABLET in 1 BOTTLE (71335-1938-3)Jun 3, 2022
71335-1938-460 TABLET in 1 BOTTLE (71335-1938-4)Sep 26, 2022
71335-1938-5180 TABLET in 1 BOTTLE (71335-1938-5)Apr 8, 2024
71335-1938-6120 TABLET in 1 BOTTLE (71335-1938-6)Apr 8, 2024

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