NDC 70518-4052 – Buspirone Hydrochloride

Buspirone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4052

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210907
Marketed since
April 15, 2024
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
70518-4052-030 TABLET in 1 BLISTER PACK (70518-4052-0)Apr 15, 2024
70518-4052-230 TABLET in 1 BLISTER PACK (70518-4052-2)Feb 12, 2025
70518-4052-390 TABLET in 1 BOTTLE, PLASTIC (70518-4052-3)Jun 18, 2025
70518-4052-430 TABLET in 1 BOTTLE, PLASTIC (70518-4052-4)Nov 28, 2025

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