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Rugby Famotidine

NDC 0536-1298 · Rugby Laboratories

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

0536-1298-01 — 1 BOTTLE in 1 CARTON (0536-1298-01) / 100 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-0511 — famotidine, calcium carbonate and magnesium hydroxide, 0363-0701 — Famotidine, 0363-0713 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 0363-1203 — famotidine, 0363-1899 — Famotidine, 0363-4036 — famotidine, calcium carbonate, magnesium hydroxide, 0363-4400 — Famotidine, 0363-5300 — Famotidine, 0363-9607 — Famotidine, 0527-5190 — Famotidine, 0615-8558 — Famotidine, 0615-8559 — Famotidine, 0641-6021 — Famotidine, 0641-6022 — Famotidine, 0641-6023 — Famotidine, 0832-6045 — Famotidine, 0904-5529 — Famotidine, 0904-5780 — Famotidine, 0904-7193 — Famotidine, 10267-5689 — 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.