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Ondansetron

NDC 71335-0132 · Bryant Ranch Prepack

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

Packages

71335-0132-0 60 TABLET, FILM COATED in 1 BOTTLE (71335-0132-0)

71335-0132-1 10 TABLET, FILM COATED in 1 BOTTLE (71335-0132-1)

71335-0132-2 3 TABLET, FILM COATED in 1 BOTTLE (71335-0132-2)

71335-0132-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-0132-3)

71335-0132-4 15 TABLET, FILM COATED in 1 BOTTLE (71335-0132-4)

71335-0132-5 6 TABLET, FILM COATED in 1 BOTTLE (71335-0132-5)

71335-0132-6 4 TABLET, FILM COATED in 1 BOTTLE (71335-0132-6)

71335-0132-7 90 TABLET, FILM COATED in 1 BOTTLE (71335-0132-7)

71335-0132-8 12 TABLET, FILM COATED in 1 BOTTLE (71335-0132-8)

71335-0132-9 20 TABLET, FILM COATED in 1 BOTTLE (71335-0132-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-9402 — Ondansetron Hydrochloride, 68999-555 — Ondansetron Hydrochloride, 69339-171 — Ondansetron, 69339-172 — Ondansetron, 70518-1585 — Ondansetron Hydrochloride, 70518-3511 — Ondansetron Hydrochloride, 70518-4145 — Ondansetron Hydrochloride, 70518-4245 — Ondansetron, 70518-4588 — Ondansetron, 71205-744 — Ondansetron Hydrochloride, 71335-0205 — Ondansetron Hydrochloride, 71335-0815 — ondansetron hydrochloride, 71335-1357 — Ondansetron Hydrochloride, 71335-1596 — Ondansetron Hydrochloride, 71335-1855 — Ondansetron Hydrochloride, 71610-119 — Ondansetron Hydrochloride, 71872-7068 — ONDANSETRON, 71872-7107 — Ondansetron, 71872-7140 — Ondansetron, 71872-7162 — ONDANSETRON, +154 more

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