NDC 69584-094 – Buspirone Hydrochloride

Buspirone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC69584-094

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Oxford Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078302
Marketed since
May 1, 2020
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
69584-094-0660 TABLET in 1 BOTTLE (69584-094-06)May 1, 2020
69584-094-18180 TABLET in 1 BOTTLE (69584-094-18)May 1, 2020
69584-094-50500 TABLET in 1 BOTTLE (69584-094-50)May 1, 2020

Recalls mentioning this NDC

Other Buspirone hydrochloride products