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Famotidine

NDC 43063-696 · PD-Rx Pharmaceuticals, Inc.

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

43063-696-30 — 30 TABLET in 1 BOTTLE, PLASTIC (43063-696-30)

43063-696-90 — 90 TABLET in 1 BOTTLE, PLASTIC (43063-696-90)

43063-696-93 — 180 TABLET in 1 BOTTLE, PLASTIC (43063-696-93)

43063-696-95 — 1000 TABLET in 1 BOTTLE, PLASTIC (43063-696-95)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41520-409 — famotidine, calcium carbonate and magnesium hydroxide, 41520-617 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 41520-707 — Famotidine, 41520-901 — Famotidine, 42507-141 — Famotidine, 42507-194 — Famotidine, 42507-321 — famotidine, calcium carbonate and magnesium hydroxide, 42571-433 — FAMOTIDINE, 43063-533 — Famotidine, 43063-695 — Famotidine, 43386-500 — Famotidine, 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, +401 more

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