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TopCare Acid Reducer

NDC 36800-194 · Topco Associates LLC

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

36800-194-02 — 25 BLISTER PACK in 1 CARTON (36800-194-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK

36800-194-71 — 1 BOTTLE in 1 CARTON (36800-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE

36800-194-78 — 1 BOTTLE in 1 CARTON (36800-194-78) / 100 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

29485-6522 — famotidine, calcium carbonate, and magnesium hydroxide tablet, chewable, 30142-040 — famotidine, calcium carbonate and magnesium hydroxide, 30142-194 — Famotidine, 30142-213 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 31722-017 — Famotidine, 31722-018 — Famotidine, 31722-063 — FAMOTIDINE, 31722-315 — Ibuprofen and famotidine, 36800-082 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 36800-141 — Famotidine, 36800-616 — famotidine, calcium carbonate and magnesium hydroxide, 37808-042 — Famotidine, 37808-121 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 37808-301 — Famotidine, 37808-503 — famotidine, calcium carbonate and magnesium hydroxide, 37835-161 — Famotidine, 37835-165 — Famotidine, 41163-001 — Famotidine, 41163-313 — Famotidine, 41163-321 — famotidine, calcium carbonate and 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.