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Famotidine

NDC 69238-2090 · Amneal Pharmaceuticals NY LLC

Generic nameFamotidine

Dosage formPOWDER, FOR SUSPENSION

RouteORAL

Active ingredient(s)FAMOTIDINE

Strength40 mg/5mL

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

Marketing categoryANDA

Packages

69238-2090-4 — 50 mL in 1 BOTTLE (69238-2090-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-4144 — Famotidine, 68788-8485 — FAMOTIDINE, 68788-8518 — FAMOTIDINE, 68788-8733 — Famotidine, 68788-8889 — Famotidine, 68788-8897 — Ibuprofen and famotidine, 69168-443 — Famotidine, 69168-445 — Famotidine, 69230-326 — famotidine, 69230-327 — famotidine, 69256-002 — Famotidine, 69306-266 — Ibuprofen and famotidine, 69367-400 — Famotidine, 69367-401 — Famotidine, 69842-063 — Famotidine, 69842-087 — Famotidine, 69842-659 — famotidine, 69842-924 — Famotidine, 69842-928 — Famotidine, 70000-0048 — 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