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Ibuprofen

NDC 80425-0243 · Advanced Rx Pharmacy of Tennessee, LLC

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength800 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

80425-0243-4 — 100 TABLET, FILM COATED in 1 BOTTLE (80425-0243-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

79903-326 — acetaminophen, ibuprofen, 79903-415 — Ibuprofen, 79903-931 — Acetaminophen and Ibuprofen (NSAID), 80267-604 — Ibuprofen, 80267-999 — Ibuprofen, 80425-0046 — Ibuprofen, 80425-0047 — Ibuprofen, 80425-0089 — Ibuprofen, 80425-0132 — Ibuprofen, 80425-0154 — Ibuprofen, 80425-0384 — Ibuprofen and famotidine, 80425-0393 — Ibuprofen, 80425-0422 — Ibuprofen and famotidine, 80425-0424 — Ibuprofen, 80425-0426 — Ibuprofen, 80425-0483 — Ibuprofen and famotidine, 80425-0537 — ibuprofen, 80425-0553 — Ibuprofen, 80425-0587 — Ibuprofen and Famotidine, 81033-019 — 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.