Famotidine
NDC 70954-316 · ANI Pharmaceuticals, Inc.
Generic nameFamotidine
Dosage formPOWDER, FOR SUSPENSION
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength40 mg/5mL
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA
Packages
70954-316-10 — 50 mL in 1 BOTTLE (70954-316-10)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
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, 70771-1702 — Famotidine, 70771-1703 — Famotidine, 70771-1924 — Ibuprofen and Famotidine, 71205-257 — Famotidine, 71205-276 — Famotidine, 71205-535 — Famotidine, 71205-634 — Famotidine, 71205-637 — Famotidine, 71205-663 — Famotidine, 71205-781 — Famotidine, 71335-0231 — Famotidine, 71335-0370 — Famotidine, 71335-0409 — Famotidine, +401 more