NDC 0093-5200 – Buspirone Hydrochloride

Buspirone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-5200

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075022
Marketed since
March 26, 2004
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0093-5200-05500 TABLET in 1 BOTTLE (0093-5200-05)Mar 26, 2004
0093-5200-0660 TABLET in 1 BOTTLE (0093-5200-06)Mar 26, 2004

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