NDC 70518-3686 – Buspirone Hydrochloride

Buspirone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-3686

Product details

Brand name
Buspirone Hydrochloride
Generic name
Buspirone Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210907
Marketed since
March 20, 2023
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
70518-3686-030 TABLET in 1 BLISTER PACK (70518-3686-0)Mar 20, 2023
70518-3686-130 TABLET in 1 BOTTLE, PLASTIC (70518-3686-1)Jun 19, 2025
70518-3686-290 TABLET in 1 BOTTLE, PLASTIC (70518-3686-2)Aug 22, 2025
70518-3686-330 TABLET in 1 BLISTER PACK (70518-3686-3)Mar 6, 2026
70518-3686-450 POUCH in 1 BOX (70518-3686-4) / 1 TABLET in 1 POUCH (70518-3686-5)Apr 23, 2026

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