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Famotidine

NDC 70771-1702 · Zydus Lifesciences Limited

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

70771-1702-0 — 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1702-0)

70771-1702-1 — 100 TABLET, FILM COATED in 1 BOTTLE (70771-1702-1)

70771-1702-3 — 30 TABLET, FILM COATED in 1 BOTTLE (70771-1702-3)

70771-1702-4 — 10 BLISTER PACK in 1 CARTON (70771-1702-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1702-2)

70771-1702-5 — 500 TABLET, FILM COATED in 1 BOTTLE (70771-1702-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4395 — Famotidine, 70518-4574 — FAMOTIDINE, 70518-4580 — Ibuprofen and famotidine, 70677-1100 — famotidine, calcium carbonate and magnesium hydroxide, 70677-1101 — Famotidine, 70677-1102 — Famotidine, 70710-1683 — Famotidine, 70710-1684 — Famotidine, 70756-051 — Famotidine, 70756-052 — Famotidine, 70771-1703 — Famotidine, 70771-1924 — Ibuprofen and Famotidine, 70954-316 — Famotidine, 71205-257 — Famotidine, 71205-276 — Famotidine, 71205-535 — Famotidine, 71205-634 — Famotidine, 71205-637 — Famotidine, 71205-663 — Famotidine, 71205-781 — 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.