NDC 71335-1605 – Buspirone Hydrochloride

Buspirone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1605

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204582
Marketed since
June 29, 2012
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-1605-130 TABLET in 1 BOTTLE (71335-1605-1)May 20, 2024
71335-1605-2100 TABLET in 1 BOTTLE (71335-1605-2)May 20, 2024
71335-1605-360 TABLET in 1 BOTTLE (71335-1605-3)May 29, 2020
71335-1605-490 TABLET in 1 BOTTLE (71335-1605-4)May 27, 2020
71335-1605-5120 TABLET in 1 BOTTLE (71335-1605-5)May 20, 2024
71335-1605-628 TABLET in 1 BOTTLE (71335-1605-6)May 20, 2024
71335-1605-7180 TABLET in 1 BOTTLE (71335-1605-7)May 20, 2024

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