NDC 71610-962 – Buspirone hydrochloride

Buspirone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-962

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, 2027

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71610-962-5360 TABLET in 1 BOTTLE (71610-962-53)Nov 5, 2025
71610-962-6090 TABLET in 1 BOTTLE (71610-962-60)Oct 31, 2025
71610-962-70120 TABLET in 1 BOTTLE (71610-962-70)Jan 8, 2026
71610-962-80180 TABLET in 1 BOTTLE (71610-962-80)Nov 5, 2025
71610-962-92270 TABLET in 1 BOTTLE (71610-962-92)Jan 8, 2026

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