NDC 68071-3713 – Ondansetron

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

Human Prescription Drug

Product NDC68071-3713

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
April 6, 2021
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (1)

Package NDCDescriptionSince
68071-3713-330 TABLET, FILM COATED in 1 BOTTLE (68071-3713-3)Oct 25, 2024

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