NDC 59651-392 – Buspirone Hydrochloride

Buspirone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC59651-392

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078246
Marketed since
February 21, 2020
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
59651-392-01100 TABLET in 1 BOTTLE (59651-392-01)Feb 21, 2020
59651-392-05500 TABLET in 1 BOTTLE (59651-392-05)Feb 21, 2020
59651-392-1010 BLISTER PACK in 1 CARTON (59651-392-10) / 10 TABLET in 1 BLISTER PACKFeb 21, 2020
59651-392-18180 TABLET in 1 BOTTLE (59651-392-18)Feb 21, 2020
59651-392-3030 TABLET in 1 BOTTLE (59651-392-30)Feb 21, 2020
59651-392-6060 TABLET in 1 BOTTLE (59651-392-60)Feb 21, 2020

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