Skip to main content

Acid Controller

NDC 0363-0701 · Walgreen Company

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

0363-0701-82 — 1 BOTTLE in 1 CARTON (0363-0701-82) / 200 TABLET, FILM COATED in 1 BOTTLE

0363-0701-98 — 1 BOTTLE in 1 CARTON (0363-0701-98) / 75 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0113-0194 — Famotidine, 0113-6023 — famotidine, calcium carbonate and magnesium hydroxide, 0113-7050 — famotidine, calcium carbonate, magnesium hydroxide, 0172-5728 — Famotidine, 0172-5729 — Famotidine, 0187-4420 — famotidine, 0187-4440 — famotidine, 0338-5197 — Famotidine, 0363-0141 — Famotidine, 0363-0511 — famotidine, calcium carbonate and magnesium hydroxide, 0363-0713 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 0363-1203 — famotidine, 0363-1899 — Famotidine, 0363-4036 — famotidine, calcium carbonate, magnesium hydroxide, 0363-4400 — Famotidine, 0363-5300 — Famotidine, 0363-9607 — Famotidine, 0527-5190 — Famotidine, 0536-1298 — Famotidine, 0615-8558 — 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.