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Famotidine

NDC 0172-5728 · Teva Pharmaceuticals USA, 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

0172-5728-60 — 100 TABLET, FILM COATED in 1 BOTTLE (0172-5728-60)

0172-5728-70 — 500 TABLET, FILM COATED in 1 BOTTLE (0172-5728-70)

0172-5728-80 — 1000 TABLET, FILM COATED in 1 BOTTLE (0172-5728-80)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0113-0032 — famotidine, calcium carbonate and magnesium hydroxide, 0113-0141 — Famotidine, 0113-0194 — Famotidine, 0113-6023 — famotidine, calcium carbonate and magnesium hydroxide, 0113-7050 — famotidine, calcium carbonate, magnesium hydroxide, 0172-5729 — Famotidine, 0187-4420 — famotidine, 0187-4440 — famotidine, 0338-5197 — Famotidine, 0363-0141 — Famotidine, 0363-0511 — famotidine, calcium carbonate and magnesium hydroxide, 0363-0701 — Famotidine, 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, +401 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.