NDC 70518-1585 – Ondansetron Hydrochloride

Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-1585

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
October 24, 2018
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
70518-1585-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-1585-0)Oct 24, 2018
70518-1585-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-1)Jan 6, 2021
70518-1585-620 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-6)Oct 1, 2025

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