NDC 29300-246 – Buspirone Hydrochloride

Buspirone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC29300-246

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
November 14, 2019
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
29300-246-01100 TABLET in 1 BOTTLE, PLASTIC (29300-246-01)Nov 20, 2019
29300-246-05500 TABLET in 1 BOTTLE, PLASTIC (29300-246-05)Nov 20, 2019
29300-246-1660 TABLET in 1 BOTTLE, PLASTIC (29300-246-16)Nov 20, 2019
29300-246-18180 TABLET in 1 BOTTLE, PLASTIC (29300-246-18)Nov 20, 2019

Recalls mentioning this NDC

Other Buspirone hydrochloride products