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ondansetron hydrochloride

NDC 55111-155 · Dr. Reddy's Laboratories Limited

Generic nameondansetron hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength16 mg/1
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

55111-155-05 — 500 TABLET, FILM COATED in 1 BOTTLE (55111-155-05)

55111-155-30 — 30 TABLET, FILM COATED in 1 BOTTLE (55111-155-30)

55111-155-78 — 10 BLISTER PACK in 1 CARTON (55111-155-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-155-79)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51662-1245 — ONDANSETRON, 51662-1366 — ONDANSETRON, 51662-1377 — ONDANSETRON, 51662-1469 — ONDANSETRON, 51662-1539 — ONDANSETRON, 51662-1678 — ONDANSETRON, 54348-819 — ONDANSETRON, 54348-821 — Ondansetron Hydrochloride, 55111-153 — ONDANSETRON HYDROCHLORIDE, 55111-154 — ONDANSETRON HYDROCHLORIDE, 55111-156 — ONDANSETRON HYDROCHLORIDE, 55150-125 — Ondansetron Hydrochloride, 55150-126 — Ondansetron Hydrochloride, 55154-2876 — Ondansetron, 55154-2877 — Ondansetron, 55154-3551 — ondansetron hydrochloride, 55154-4453 — ONDANSETRON HYDROCHLORIDE, 55154-6976 — ONDANSETRON, 55154-7879 — ondansetron hydrochloride, 55700-627 — Ondansetron Hydrochloride, +154 more

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