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Ondansetron

NDC 68071-4834 · NuCare Pharmaceuticals,Inc.

Generic nameOndansetron
Dosage formTABLET, ORALLY DISINTEGRATING
RouteORAL
Active ingredient(s)ONDANSETRON
Strength4 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

68071-4834-1 — 10 TABLET, ORALLY DISINTEGRATING in 1 BOX (68071-4834-1)

68071-4834-2 — 2 TABLET, ORALLY DISINTEGRATING in 1 BOX (68071-4834-2)

68071-4834-4 — 4 TABLET, ORALLY DISINTEGRATING in 1 BOX (68071-4834-4)

68071-4834-6 — 6 TABLET, ORALLY DISINTEGRATING in 1 BOX (68071-4834-6)

68071-4834-7 — 20 TABLET, ORALLY DISINTEGRATING in 1 BOX (68071-4834-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68001-247 — Ondansetron, 68071-1730 — Ondansetron, 68071-2284 — ondansetron, 68071-2718 — Ondansetron, 68071-2763 — Ondansetron, 68071-2901 — Ondansetron, 68071-3268 — Ondansetron, 68071-3926 — Ondansetron, 68071-4115 — Ondansetron, 68071-4570 — Ondansetron, 68071-4881 — Ondansetron, 68071-5021 — Ondansetron, 68071-5167 — Ondansetron, 68071-5230 — ondansetron, 68462-157 — Ondansetron, 68462-158 — Ondansetron, 68788-4133 — Ondansetron, 68788-7565 — Ondansetron, 68788-7644 — Ondansetron, 68788-8666 — Ondansetron, +78 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.