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foster and thrive acid reducer

NDC 70677-1102 · Strategic Sourcing Services LLC

Generic nameFamotidine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength10 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

70677-1102-1 — 30 BLISTER PACK in 1 CARTON (70677-1102-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK

70677-1102-2 — 1 BOTTLE in 1 CARTON (70677-1102-2) / 60 TABLET, FILM COATED in 1 BOTTLE

70677-1102-3 — 1 BOTTLE in 1 CARTON (70677-1102-3) / 90 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70264-034 — famotidine, calcium carbonate, and magnesium hydroxide, 70377-113 — FAMOTIDINE, 70518-3829 — 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, 70710-1683 — Famotidine, 70710-1684 — Famotidine, 70756-051 — Famotidine, 70756-052 — Famotidine, 70771-1702 — Famotidine, 70771-1703 — Famotidine, 70771-1924 — Ibuprofen and Famotidine, 70954-316 — Famotidine, 71205-257 — Famotidine, 71205-276 — 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.