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Ondansetron

NDC 83980-013 · Ipca Laboratories Limited

Generic nameOndansetron
Dosage formTABLET, ORALLY DISINTEGRATING
RouteORAL
Active ingredient(s)ONDANSETRON
Strength8 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

83980-013-01 — 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (83980-013-01)

83980-013-10 — 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (83980-013-10)

83980-013-13 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (83980-013-13)

83980-013-83 — 3 BLISTER PACK in 1 CARTON (83980-013-83) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2972 — Ondansetron, 71335-2973 — Ondansetron, 71335-2974 — Ondansetron, 71335-3073 — Ondansetron, 71335-9726 — Ondansetron, 72336-073 — Ondansetron, 76420-056 — Ondansetron, 76420-217 — Ondansetron, 76420-251 — Ondansetron, 80425-0073 — Ondansetron, 80425-0222 — Ondansetron, 80425-0227 — Ondansetron, 80425-0228 — Ondansetron, 80425-0469 — Ondansetron, 80425-0473 — Ondansetron, 83980-012 — Ondansetron, 85534-0025 — Ondansetron, 85534-0063 — Ondansetron, 85766-038 — Ondansetron, 85766-213 — 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.