NDC 0615-7689 – Buspirone Hydrochloride

Buspirone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC0615-7689

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075022
Marketed since
March 1, 2002
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0615-7689-0515 TABLET in 1 BLISTER PACK (0615-7689-05)Nov 30, 2022
0615-7689-3930 TABLET in 1 BLISTER PACK (0615-7689-39)Jan 24, 2013

Recalls mentioning this NDC

Other Buspirone hydrochloride products