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Ibuprofen

NDC 53345-059 · Humanwell PuraCap Pharmaceuticals (Wuhan) Co., Ltd

Generic nameibuprofen
Dosage formCAPSULE, LIQUID FILLED
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

53345-059-01 — 1 BAG in 1 CARTON (53345-059-01) / 12000 CAPSULE, LIQUID FILLED in 1 BAG

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53041-634 — Ibuprofen, 53041-637 — Ibuprofen, 53041-638 — Ibuprofen, 53041-639 — Ibuprofen, 53185-381 — Ibuprofen 200mg, 53209-2001 — Ibuprofen, 53329-674 — Ibuprofen, 53345-014 — Ibuprofen, 53345-039 — Ibuprofen, 53345-050 — Ibuprofen mini, 53746-116 — Hydrocodone Bitartrate and Ibuprofen, 53746-117 — Hydrocodone Bitartrate and Ibuprofen, 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, +1311 more

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