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Famotidine

NDC 46708-294 · Alembic Pharmaceuticals Limited

Generic nameFamotidine
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength40 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

46708-294-10 — 100 TABLET in 1 CARTON (46708-294-10)

46708-294-30 — 30 TABLET in 1 BOTTLE (46708-294-30)

46708-294-31 — 100 TABLET in 1 BOTTLE (46708-294-31)

46708-294-71 — 500 TABLET in 1 BOTTLE (46708-294-71)

46708-294-91 — 1000 TABLET in 1 BOTTLE (46708-294-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43598-572 — Famotidine, 43598-824 — Famotidine, 43598-960 — Famotidine, 43602-511 — Famotidine, 43602-544 — Ibuprofen and famotidine, 43602-602 — Famotidine, 46122-345 — famotidine, calcium carbonate and magnesium hydroxide, 46122-735 — Famotidine, 46122-737 — Famotidine, 46708-293 — Famotidine, 48433-150 — Famotidine, 49035-321 — famotidine, calcium carbonate and magnesium hydroxide, 49035-505 — Famotidine, 49035-507 — Famotidine, 49035-546 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 49035-589 — Famotidine, 49035-650 — Famotidine, 49483-720 — Famotidine, 49884-366 — Ibuprofen and famotidine, 50090-1044 — 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.