NDC 71335-2237 – Buspirone hydrochloride

Buspirone Hydrochloride 7.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2237

Product details

Brand name
Buspirone hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078888
Marketed since
March 21, 2023
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-2237-130 TABLET in 1 BOTTLE (71335-2237-1)Apr 3, 2024
71335-2237-290 TABLET in 1 BOTTLE (71335-2237-2)Aug 29, 2023
71335-2237-318 TABLET in 1 BOTTLE (71335-2237-3)Apr 3, 2024
71335-2237-428 TABLET in 1 BOTTLE (71335-2237-4)Apr 3, 2024
71335-2237-560 TABLET in 1 BOTTLE (71335-2237-5)Apr 3, 2024
71335-2237-6120 TABLET in 1 BOTTLE (71335-2237-6)Apr 3, 2024

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