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IBUPROFEN

NDC 49483-601 · TIME CAP LABORATORIES,INC

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 categoryANDA

Packages

49483-601-00 — 6500 TABLET, FILM COATED in 1 BAG (49483-601-00)

49483-601-01 — 100 TABLET, FILM COATED in 1 BOTTLE (49483-601-01)

49483-601-05 — 50 TABLET, FILM COATED in 1 BOTTLE (49483-601-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49035-670 — IBUPROFEN, DIPHENHYDRAMINE HCL, 49035-693 — Ibuprofen, 49035-699 — diphenhydramine citrate, ibuprofen, 49035-897 — Ibuprofen, 49035-912 — Ibuprofen, 49314-0993 — Ibuprofen, 49314-1003 — Ibuprofen, 49483-114 — Ibuprofen, 49483-133 — Ibuprofen Capsules 200 mg, 49483-600 — IBUPFROFEN, 49483-602 — Ibuprofen, 49483-603 — Ibuprofen, 49483-604 — Ibuprofen, 49483-610 — IBUPROFEN, 49483-611 — IBUPROFEN, 49483-612 — IBUPROFEN, 49483-700 — Ibuprofen, 49483-716 — Acetaminophen, Ibuprofen, 49884-366 — Ibuprofen and famotidine, 50090-2549 — 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.