NDC 71335-2576 – Buspirone Hydrochloride

Buspirone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2576

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
October 17, 2023
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-2576-130 TABLET in 1 BOTTLE (71335-2576-1)Feb 5, 2025
71335-2576-2100 TABLET in 1 BOTTLE (71335-2576-2)Feb 5, 2025
71335-2576-360 TABLET in 1 BOTTLE (71335-2576-3)Feb 5, 2025
71335-2576-490 TABLET in 1 BOTTLE (71335-2576-4)Feb 5, 2025
71335-2576-5120 TABLET in 1 BOTTLE (71335-2576-5)Feb 5, 2025
71335-2576-628 TABLET in 1 BOTTLE (71335-2576-6)Feb 5, 2025
71335-2576-7180 TABLET in 1 BOTTLE (71335-2576-7)Feb 5, 2025

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