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Ondansetron Hydrochloride

NDC 71335-1596 · Bryant Ranch Prepack

Generic nameOndansetron Hydrochloride
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

71335-1596-0 60 TABLET, FILM COATED in 1 BOTTLE (71335-1596-0)

71335-1596-1 10 TABLET, FILM COATED in 1 BOTTLE (71335-1596-1)

71335-1596-2 3 TABLET, FILM COATED in 1 BOTTLE (71335-1596-2)

71335-1596-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-1596-3)

71335-1596-4 15 TABLET, FILM COATED in 1 BOTTLE (71335-1596-4)

71335-1596-5 6 TABLET, FILM COATED in 1 BOTTLE (71335-1596-5)

71335-1596-6 4 TABLET, FILM COATED in 1 BOTTLE (71335-1596-6)

71335-1596-7 90 TABLET, FILM COATED in 1 BOTTLE (71335-1596-7)

71335-1596-8 12 TABLET, FILM COATED in 1 BOTTLE (71335-1596-8)

71335-1596-9 20 TABLET, FILM COATED in 1 BOTTLE (71335-1596-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-1585 — Ondansetron Hydrochloride, 70518-3511 — Ondansetron Hydrochloride, 70518-4145 — Ondansetron Hydrochloride, 70518-4245 — Ondansetron, 70518-4588 — Ondansetron, 71205-744 — Ondansetron Hydrochloride, 71335-0132 — Ondansetron, 71335-0205 — Ondansetron Hydrochloride, 71335-0815 — ondansetron hydrochloride, 71335-1357 — Ondansetron Hydrochloride, 71335-1855 — Ondansetron Hydrochloride, 71610-119 — Ondansetron Hydrochloride, 71872-7068 — ONDANSETRON, 71872-7107 — Ondansetron, 71872-7140 — Ondansetron, 71872-7162 — ONDANSETRON, 72162-2364 — Ondansetron Hydrochloride, 72162-2365 — Ondansetron Hydrochloride, 72266-123 — Ondansetron, 72266-124 — 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.