NDC 65841-781 – Buspirone hydrochloride

Buspirone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC65841-781

Product details

Brand name
Buspirone hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078888
Marketed since
May 3, 2014
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
65841-781-01100 TABLET in 1 BOTTLE (65841-781-01)May 3, 2014
65841-781-05500 TABLET in 1 BOTTLE (65841-781-05)May 3, 2014
65841-781-101000 TABLET in 1 BOTTLE (65841-781-10)May 3, 2014
65841-781-77100 BLISTER PACK in 1 CARTON (65841-781-77) / 1 TABLET in 1 BLISTER PACK (65841-781-30)May 3, 2014

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