NDC 82804-964 – Buspirone Hydrochloride

Buspirone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-964

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078302
Marketed since
May 1, 2020
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
82804-964-00100 TABLET in 1 BOTTLE (82804-964-00)Jan 12, 2026
82804-964-111000 TABLET in 1 BOTTLE (82804-964-11)Jan 12, 2026
82804-964-3030 TABLET in 1 BOTTLE (82804-964-30)Jan 12, 2026
82804-964-55500 TABLET in 1 BOTTLE (82804-964-55)Jan 12, 2026
82804-964-6060 TABLET in 1 BOTTLE (82804-964-60)Jan 12, 2026
82804-964-72120 TABLET in 1 BOTTLE (82804-964-72)Jan 12, 2026
82804-964-9090 TABLET in 1 BOTTLE (82804-964-90)Jan 12, 2026

Other Buspirone hydrochloride products