NDC 71335-0007 – Buspirone Hydrochloride

Buspirone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0007

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202557
Marketed since
December 15, 2016
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-0007-130 TABLET in 1 BOTTLE (71335-0007-1)May 14, 2026
71335-0007-260 TABLET in 1 BOTTLE (71335-0007-2)May 14, 2026
71335-0007-390 TABLET in 1 BOTTLE (71335-0007-3)May 14, 2026
71335-0007-445 TABLET in 1 BOTTLE (71335-0007-4)May 14, 2026
71335-0007-5180 TABLET in 1 BOTTLE (71335-0007-5)May 14, 2026
71335-0007-6120 TABLET in 1 BOTTLE (71335-0007-6)May 14, 2026
71335-0007-710 TABLET in 1 BOTTLE (71335-0007-7)May 14, 2026
71335-0007-8100 TABLET in 1 BOTTLE (71335-0007-8)May 14, 2026

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