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Famotidine

NDC 71205-535 · Proficient Rx LP

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

71205-535-06 — 6 TABLET, FILM COATED in 1 BOTTLE (71205-535-06)

71205-535-10 — 10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)

71205-535-30 — 30 TABLET, FILM COATED in 1 BOTTLE (71205-535-30)

71205-535-60 — 60 TABLET, FILM COATED in 1 BOTTLE (71205-535-60)

71205-535-78 — 180 TABLET, FILM COATED in 1 BOTTLE (71205-535-78)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70710-1683 — Famotidine, 70710-1684 — Famotidine, 70756-051 — Famotidine, 70756-052 — Famotidine, 70771-1702 — Famotidine, 70771-1703 — Famotidine, 70771-1924 — Ibuprofen and Famotidine, 70954-316 — Famotidine, 71205-257 — Famotidine, 71205-276 — Famotidine, 71205-634 — Famotidine, 71205-637 — Famotidine, 71205-663 — Famotidine, 71205-781 — Famotidine, 71335-0231 — Famotidine, 71335-0370 — Famotidine, 71335-0409 — Famotidine, 71335-1520 — Famotidine, 71335-1950 — Famotidine, 71335-2190 — 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.