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Ibuprofen

NDC 53746-460 · Amneal Pharmaceuticals of New York LLC

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

Packages

53746-460-02 — 250 TABLET in 1 BOTTLE (53746-460-02)

53746-460-10 — 1000 TABLET in 1 BOTTLE (53746-460-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53746-131 — Ibuprofen, 53746-132 — Ibuprofen, 53746-137 — Ibuprofen, 53746-140 — Ibuprofen, 53746-142 — Ibuprofen, 53746-143 — Ibuprofen, 53746-144 — Ibuprofen, 53746-145 — Hydrocodone Bitartrate and Ibuprofen, 53746-146 — Hydrocodone Bitartrate and Ibuprofen, 53746-458 — Ibuprofen, 53746-462 — Ibuprofen, 53746-464 — Ibuprofen, 53746-465 — Ibuprofen, 53746-466 — Ibuprofen, 53942-112 — Ibuprofen, 53942-119 — IBUPROFEN, 53943-034 — Acetaminophen and Ibuprofen, 53943-111 — Ibuprofen, 53943-112 — Ibuprofen, 53943-119 — 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.