NDC 0615-7714 – Buspirone Hydrochloride

Buspirone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC0615-7714

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
February 28, 2002
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0615-7714-0515 TABLET in 1 BLISTER PACK (0615-7714-05)Nov 21, 2022
0615-7714-306 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7714-30) / 5 TABLET in 1 BLISTER PACKApr 23, 2012
0615-7714-3930 TABLET in 1 BLISTER PACK (0615-7714-39)Apr 23, 2012

Recalls mentioning this NDC

Other Buspirone hydrochloride products