NDC 71335-1752 – Buspirone Hydrochloride

Buspirone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1752

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075388
Marketed since
July 27, 2020
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-1752-130 TABLET in 1 BOTTLE (71335-1752-1)Apr 22, 2021
71335-1752-2100 TABLET in 1 BOTTLE (71335-1752-2)Dec 31, 2020
71335-1752-360 TABLET in 1 BOTTLE (71335-1752-3)Feb 4, 2021
71335-1752-490 TABLET in 1 BOTTLE (71335-1752-4)Apr 12, 2021
71335-1752-5120 TABLET in 1 BOTTLE (71335-1752-5)Dec 10, 2021
71335-1752-628 TABLET in 1 BOTTLE (71335-1752-6)May 3, 2022
71335-1752-7180 TABLET in 1 BOTTLE (71335-1752-7)Mar 1, 2022

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