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Famotidine 10 mg

NDC 25000-086 · MARKSANS PHARMA LIMITED

Generic nameFamotidine 10 mg
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength10 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

25000-086-03 — 1 BOTTLE in 1 CARTON (25000-086-03) / 30 TABLET, COATED in 1 BOTTLE

25000-086-07 — 1 BOTTLE in 1 CARTON (25000-086-07) / 90 TABLET, COATED in 1 BOTTLE

25000-086-08 — 1 BOTTLE in 1 CARTON (25000-086-08) / 100 TABLET, COATED in 1 BOTTLE

25000-086-36 — 3 BLISTER PACK in 1 CARTON (25000-086-36) / 10 TABLET, COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21130-039 — Famotidine, 21130-087 — famotidine, calcium carbonate and magnesium hydroxide, 21130-191 — Famotidine, 21130-249 — Famotidine, 21130-521 — Famotidine, 21130-546 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 21130-614 — famotidine, calcium carbonate and magnesium hydroxide, 21130-771 — Famotidine, 21130-777 — Famotidine, 21130-786 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 25000-087 — Famotidine 20 mg, 25000-124 — Famotidine 20 mg, 25021-753 — Famotidine, 25021-754 — Famotidine, 25021-755 — Famotidine, 25021-756 — Famotidine, 27241-249 — Famotidine, 29485-6522 — famotidine, calcium carbonate, and magnesium hydroxide tablet, chewable, 30142-040 — famotidine, calcium carbonate and magnesium hydroxide, 30142-194 — 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.