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Ibuprofen

NDC 43063-867 · PD-Rx Pharmaceuticals, Inc.

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength600 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

43063-867-01 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-01)

43063-867-10 — 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-10)

43063-867-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-30)

43063-867-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-867-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42507-909 — Ibuprofen, 42543-964 — Ibuprofen, 42543-965 — Ibuprofen, 42543-966 — Ibuprofen, 42681-0026 — Ibuprofen, 42681-0052 — Ibuprofen, 42681-0061 — IBUPROFEN AND DIPHENHYDRAMINE HCL, 42708-097 — Ibuprofen, 42708-175 — Ibuprofen, 42961-203 — Ibuprofen, 43063-872 — Ibuprofen, 43063-914 — Ibuprofen, 43598-052 — Acetaminophen and Ibuprofen, 43602-544 — Ibuprofen and famotidine, 45802-133 — Ibuprofen, 45802-140 — Ibuprofen, 45802-897 — Ibuprofen, 45802-952 — Ibuprofen, 46122-548 — Ibuprofen, 46122-580 — 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.