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IBUPROFEN AND FAMOTIDINE

NDC 85509-1315 · PHOENIX RX LLC

Generic nameIbuprofen and famotidine
Dosage formTABLET
RouteORAL
Active ingredient(s)IBUPROFEN, FAMOTIDINE
Strength26.6; 800 mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

85509-1315-3 — 30 TABLET in 1 BOTTLE (85509-1315-3)

85509-1315-6 — 60 TABLET in 1 BOTTLE (85509-1315-6)

85509-1315-9 — 90 TABLET in 1 BOTTLE (85509-1315-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

84324-038 — Ibuprofen, 84324-039 — Ibuprofen, 85237-1784 — diphenhydramine citrate and ibuprofen, 85237-1785 — ibuprofen, 85237-1786 — ibuprofen, 85237-1886 — Ibuprofen, Acetaminophen, 85237-1926 — Famotidine, 85237-1947 — Ibuprofen, 85237-1948 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 85509-1010 — Ibuprofen and famotidine, 85509-1466 — Ibuprofen, 85509-1626 — Ibuprofen and famotidine, 85509-2396 — Ibuprofen, 85534-0011 — Ibuprofen, 85534-0012 — Ibuprofen, 85534-0013 — Ibuprofen, 85534-0091 — FAMOTIDINE, 85534-0092 — FAMOTIDINE, 85576-101 — acetaminophen, ibuprofen, 85766-044 — Acetaminophen, Ibuprofen, +1712 more

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