Skip to main content

FAMOTIDINE

NDC 43602-602 · Ascent Pharmaceuticals, Inc.

Generic nameFamotidine
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

43602-602-03 — 1 BOTTLE in 1 CARTON (43602-602-03) / 300 TABLET in 1 BOTTLE

43602-602-30 — 1 BOTTLE in 1 CARTON (43602-602-30) / 30 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42571-433 — FAMOTIDINE, 43063-533 — Famotidine, 43063-695 — Famotidine, 43063-696 — Famotidine, 43386-500 — Famotidine, 43598-572 — Famotidine, 43598-824 — Famotidine, 43598-960 — Famotidine, 43602-511 — Famotidine, 43602-544 — Ibuprofen and famotidine, 46122-345 — famotidine, calcium carbonate and magnesium hydroxide, 46122-735 — Famotidine, 46122-737 — Famotidine, 46708-293 — Famotidine, 46708-294 — 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, +401 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.