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Famotidine

NDC 71821-012 · VKT Pharma Private Limited

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameFamotidine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength10 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

71821-012-08 — 288461 TABLET, FILM COATED in 1 BAG (71821-012-08)

71821-012-09 — 288461 TABLET, FILM COATED in 1 BAG (71821-012-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2190 — Famotidine, 71335-2442 — FAMOTIDINE, 71335-2527 — Famotidine, 71335-2805 — Famotidine, 71335-9615 — Famotidine, 71335-9724 — FAMOTIDINE, 71335-9748 — FAMOTIDINE, 71610-399 — Famotidine, 71610-470 — Famotidine, 71821-010 — Famotidine, 71872-7220 — Famotidine, 71872-7235 — Famotidine, 71872-7366 — Famotidine, 72036-026 — Famotidine, 72162-1737 — Famotidine, 72162-2599 — FAMOTIDINE, 72189-141 — FAMOTIDINE, 72189-207 — FAMOTIDINE, 72189-543 — Famotidine, 72189-641 — Ibuprofen 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.