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Acid Controller

NDC 37808-042 · H E B

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

37808-042-63 — 1 BOTTLE in 1 CARTON (37808-042-63) / 25 TABLET, FILM COATED in 1 BOTTLE

37808-042-71 — 1 BOTTLE in 1 CARTON (37808-042-71) / 50 TABLET, FILM COATED in 1 BOTTLE

37808-042-82 — 1 BOTTLE in 1 CARTON (37808-042-82) / 200 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 36800-194 — Famotidine, 36800-616 — famotidine, calcium carbonate and magnesium hydroxide, 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, 41167-0361 — Famotidine, 41167-0364 — 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.