NDC 65841-782 – buspirone hydrochloride

Buspirone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC65841-782

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
65841-782-01100 TABLET in 1 BOTTLE (65841-782-01)May 3, 2014
65841-782-05500 TABLET in 1 BOTTLE (65841-782-05)May 3, 2014
65841-782-101000 TABLET in 1 BOTTLE (65841-782-10)May 3, 2014
65841-782-77100 BLISTER PACK in 1 CARTON (65841-782-77) / 1 TABLET in 1 BLISTER PACK (65841-782-30)May 3, 2014

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