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FAMOTIDINE

NDC 70518-3829 · REMEDYREPACK 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

70518-3829-1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-1)

70518-3829-3 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-3)

70518-3829-4 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-4)

70518-3829-5 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-5)

70518-3829-6 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-6)

70518-3829-7 60 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-7)

70518-3829-8 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-8)

70518-3829-9 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-924 — Famotidine, 69842-928 — Famotidine, 70000-0048 — Famotidine, 70000-0049 — Famotidine, 70000-0416 — Famotidine, Calcium Carbonate, Magnesium Hydroxide, 70000-0582 — famotidine, calcium carbonate and magnesium hydroxide, 70000-0654 — Famotidine, 70000-0710 — Famotidine, 70264-034 — famotidine, calcium carbonate, and magnesium hydroxide, 70377-113 — FAMOTIDINE, 70518-4084 — FAMOTIDINE, 70518-4394 — Famotidine, 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, +401 more

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