NDC 71335-2073 – Buspirone Hydrochloride

Buspirone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2073

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078246
Marketed since
February 21, 2020
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-2073-130 TABLET in 1 BOTTLE (71335-2073-1)Apr 25, 2022
71335-2073-2100 TABLET in 1 BOTTLE (71335-2073-2)Apr 25, 2022
71335-2073-360 TABLET in 1 BOTTLE (71335-2073-3)Apr 25, 2022
71335-2073-490 TABLET in 1 BOTTLE (71335-2073-4)Apr 25, 2022
71335-2073-5120 TABLET in 1 BOTTLE (71335-2073-5)Apr 25, 2022
71335-2073-628 TABLET in 1 BOTTLE (71335-2073-6)Apr 25, 2022
71335-2073-7180 TABLET in 1 BOTTLE (71335-2073-7)Apr 25, 2022

Other Buspirone hydrochloride products