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Motrin IB

NDC 73097-028 · Savings Distributors LLC

Generic nameIBUPROFEN
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength200 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryNDA

Packages

73097-028-02 — 1 POUCH in 1 CARTON (73097-028-02) / 2 TABLET, FILM COATED in 1 POUCH

73097-028-40 — 20 POUCH in 1 CARTON (73097-028-40) / 2 TABLET, FILM COATED in 1 POUCH

73097-028-50 — 25 POUCH in 1 CARTON (73097-028-50) / 2 TABLET, FILM COATED in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72789-218 — Ibuprofen, 72789-363 — Ibuprofen, 72789-364 — Ibuprofen, 72789-382 — Ibuprofen, 72789-565 — Ibuprofen, 72789-584 — Ibuprofen, 72888-479 — Ibuprofen, 73086-210 — ibuprofen, 73086-211 — ibuprofen, 73086-212 — ibuprofen, 73408-509 — Ibuprofen, 73408-809 — Ibuprofen, 73598-1102 — IBUPROFEN, 73598-1104 — IBUPROFEN, 73614-201 — Ibuprofen, 75907-158 — Acetaminophen and Ibuprofen (NSAID) Tablets, 250 mg/ 125 mg, 75907-428 — Ibuprofen, 76162-501 — Acetaminophen, Ibuprofen, 76162-520 — acetaminophen, ibuprofen, 76281-119 — IBUPROFEN, +1311 more

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