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FAMOTIDINE

NDC 70518-4574 · REMEDYREPACK INC.

Generic nameFAMOTIDINE
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

70518-4574-0 — 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4574-0)

70518-4574-1 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4574-1)

70518-4574-2 — 80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4574-2)

70518-4574-3 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4574-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70000-0416 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 70000-0582 — famotidine, calcium carbonate and magnesium hydroxide, 70000-0654 — Famotidine, 70000-0710 — Famotidine, 70264-034 — famotidine, calcium carbonate, and magnesium hydroxide, 70377-113 — FAMOTIDINE, 70518-3829 — FAMOTIDINE, 70518-4084 — FAMOTIDINE, 70518-4394 — Famotidine, 70518-4395 — Famotidine, 70518-4580 — Ibuprofen and famotidine, 70677-1100 — famotidine, calcium carbonate and magnesium hydroxide, 70677-1101 — Famotidine, 70677-1102 — Famotidine, 70710-1683 — Famotidine, 70710-1684 — Famotidine, 70756-051 — Famotidine, 70756-052 — Famotidine, 70771-1702 — Famotidine, 70771-1703 — Famotidine, +401 more

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