Ranitidine

NDC 53746-254 · Amneal Pharmaceuticals of New York LLC

Generic nameRanitidine

Dosage formTABLET

RouteORAL

Active ingredient(s)RANITIDINE HYDROCHLORIDE

Strength300 mg/1

Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Marketing categoryANDA

Packages

53746-254-01 — 100 TABLET in 1 BOTTLE (53746-254-01)

53746-254-02 — 250 TABLET in 1 BOTTLE (53746-254-02)

53746-254-30 — 30 TABLET in 1 BOTTLE (53746-254-30)

FDA lists these products with the same active ingredient.

27241-109 — Ranitidine, 27241-110 — Ranitidine, 53746-253 — Ranitidine, 55111-129 — Ranitidine Hydrochloride, 55111-130 — Ranitidine Hydrochloride, 55111-131 — Ranitidine, 55111-404 — Ranitidine, 62207-773 — Ranitidine, 62207-774 — Ranitidine, 64980-636 — RANITIDINE, 64980-637 — RANITIDINE, 67091-244 — Ranitidine Hydrochloride

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