NDC 68382-183 – Buspirone hydrochloride

Buspirone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-183

Product details

Brand name
Buspirone hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078888
Marketed since
May 3, 2014
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
68382-183-05500 TABLET in 1 BOTTLE (68382-183-05)May 3, 2014
68382-183-101000 TABLET in 1 BOTTLE (68382-183-10)May 3, 2014
68382-183-1460 TABLET in 1 BOTTLE (68382-183-14)May 3, 2014
68382-183-77100 BLISTER PACK in 1 CARTON (68382-183-77) / 1 TABLET in 1 BLISTER PACK (68382-183-30)May 3, 2014

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