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Famotidine

NDC 72789-331 · PD-Rx Pharmaceuticals, Inc.

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

72789-331-02 — 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-02)

72789-331-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-20)

72789-331-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-30)

72789-331-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-60)

72789-331-90 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-90)

72789-331-93 — 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-93)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72288-774 — famotidine, calcium carbonate and magnesium hydroxide, 72476-150 — famotidine, 72476-299 — famotidine, 72559-032 — Famotidine 20 mg, 72559-038 — Famotidine, 72578-214 — Ibuprofen and Famotidine, 72603-171 — Famotidine, 72657-112 — Famotidine, 72657-113 — Famotidine, 72657-132 — Famotidine, 72789-345 — FAMOTIDINE, 72789-427 — Famotidine, 72789-453 — FAMOTIDINE, 72865-214 — Famotidine, 72865-215 — Famotidine, 73097-017 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 73581-108 — Famotidine 10mg, 73581-109 — Famotidine 20mg, 76162-300 — famotidine, 76420-712 — 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.