NDC 29300-478 – Buspirone Hydrochloride

Buspirone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC29300-478

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210907
Marketed since
October 17, 2023
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
29300-478-01100 TABLET in 1 BOTTLE, PLASTIC (29300-478-01)Dec 22, 2023
29300-478-05500 TABLET in 1 BOTTLE, PLASTIC (29300-478-05)Dec 22, 2023
29300-478-1660 TABLET in 1 BOTTLE, PLASTIC (29300-478-16)Dec 22, 2023

Recalls mentioning this NDC

Other Buspirone hydrochloride products