NDC 71610-959 – Buspirone hydrochloride

Buspirone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-959

Product details

Brand name
Buspirone hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202087
Marketed since
September 18, 2025
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71610-959-3030 TABLET in 1 BOTTLE (71610-959-30)Oct 28, 2025
71610-959-5360 TABLET in 1 BOTTLE (71610-959-53)Oct 28, 2025
71610-959-6090 TABLET in 1 BOTTLE (71610-959-60)Oct 28, 2025
71610-959-80180 TABLET in 1 BOTTLE (71610-959-80)Oct 28, 2025
71610-959-92270 TABLET in 1 BOTTLE (71610-959-92)Dec 9, 2025

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