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Famotidine

NDC 68788-4119 · Preferred Pharmaceuticals Inc.

Generic nameFamotidine
Dosage formTABLET
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

68788-4119-1 — 100 TABLET in 1 BOTTLE (68788-4119-1)

68788-4119-3 — 30 TABLET in 1 BOTTLE (68788-4119-3)

68788-4119-4 — 14 TABLET in 1 BOTTLE (68788-4119-4)

68788-4119-6 — 60 TABLET in 1 BOTTLE (68788-4119-6)

68788-4119-8 — 120 TABLET in 1 BOTTLE (68788-4119-8)

68788-4119-9 — 90 TABLET in 1 BOTTLE (68788-4119-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-4197 — Famotidine, 68094-054 — FAMOTIDINE, 68180-150 — Famotidine, 68196-121 — Famotidine, 68382-444 — famotidine, 68391-300 — Famotidine, 68475-400 — famotidine, 68645-594 — Famotidine, 68788-4021 — Famotidine, 68788-4088 — Famotidine, 68788-4144 — Famotidine, 68788-8485 — FAMOTIDINE, 68788-8518 — FAMOTIDINE, 68788-8733 — Famotidine, 68788-8889 — Famotidine, 68788-8897 — Ibuprofen and famotidine, 69168-443 — Famotidine, 69168-445 — Famotidine, 69230-326 — famotidine, 69230-327 — 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.