NDC 83980-018 – Ondansetron hydrochloride

Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC83980-018

Product details

Brand name
Ondansetron hydrochloride
Generic name
Ondansetron hydrochloride
Labeler
Ipca Laboratories Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203761
Marketed since
August 14, 2026
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
83980-018-101000 TABLET, FILM COATED in 1 BOTTLE (83980-018-10)Aug 14, 2026
83980-018-1330 TABLET, FILM COATED in 1 BOTTLE (83980-018-13)Aug 14, 2026
83980-018-9710 TABLET, FILM COATED in 1 BOTTLE (83980-018-97)Aug 14, 2026

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