NDC 71335-1144 – Buspirone Hydrochloride

Buspirone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1144

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209696
Marketed since
June 17, 2024
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-1144-130 TABLET in 1 BOTTLE (71335-1144-1)Jul 9, 2024
71335-1144-260 TABLET in 1 BOTTLE (71335-1144-2)Jul 9, 2024
71335-1144-390 TABLET in 1 BOTTLE (71335-1144-3)Jul 9, 2024
71335-1144-445 TABLET in 1 BOTTLE (71335-1144-4)Jul 9, 2024
71335-1144-5180 TABLET in 1 BOTTLE (71335-1144-5)Jul 9, 2024
71335-1144-6120 TABLET in 1 BOTTLE (71335-1144-6)Jul 9, 2024

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