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Ranitidine

NDC 27241-110 · Ajanta Pharma USA Inc.

Generic nameRanitidine
Dosage formCAPSULE
RouteORAL
Active ingredient(s)RANITIDINE HYDROCHLORIDE
Strength300 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

27241-110-03 — 30 CAPSULE in 1 BOTTLE (27241-110-03)

27241-110-10 — 100 CAPSULE in 1 BOTTLE (27241-110-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

27241-109 — Ranitidine, 53746-253 — Ranitidine, 53746-254 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels