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Migraine Relief

NDC 69452-263 · Bionpharma Inc.

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

69452-263-11 — 1 BOTTLE in 1 CARTON (69452-263-11) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE

69452-263-78 — 1 BOTTLE in 1 CARTON (69452-263-78) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE

69452-263-79 — 160 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-263-79)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69367-448 — Ibuprofen, 69367-449 — Ibuprofen, 69396-141 — Ibuprofen, 69396-145 — Ibuprofen, 69396-172 — Ibuprofen, 69452-205 — IBUPROFEN, DIPHENHYDRAMINE HCL, 69452-212 — Ibuprofen, 69452-239 — Ibuprofen, 69452-260 — Ibuprofen, 69452-262 — Ibuprofen, 69452-264 — IBUPROFEN, DIPHENHYDRAMINE HCL, 69452-302 — Ibuprofen, 69452-305 — Ibuprofen, 69452-394 — Acetaminophen and Ibuprofen, 69452-446 — Acetaminophen and Ibuprofen, 69452-447 — Acetaminophen and Ibuprofen, 69452-469 — Acetaminophen and Ibuprofen, 69452-507 — IBUPROFEN AND DIPHENHYDRAMINE HCL, 69452-513 — Ibuprofen, 69517-111 — 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.