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Ibuprofen

NDC 17856-5310 · ATLANTIC BIOLOGICALS CORP.

Generic nameIbuprofen
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)IBUPROFEN
Strength100 mg/5mL
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

17856-5310-1 — 50 CUP, UNIT-DOSE in 1 CASE (17856-5310-1) / 30 mL in 1 CUP, UNIT-DOSE

17856-5310-5 — 48 SYRINGE in 1 CASE (17856-5310-5) / 5 mL in 1 SYRINGE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-4461 — Ibuprofen, 11822-5777 — Acetaminophen, Ibuprofen, 11822-6604 — Ibuprofen, 11822-7891 — IBUPROFEN, 11822-7892 — IBUPROFEN, 11822-7893 — IBUPROFEN, 11822-8925 — IBUPROFEN, 11822-9998 — Ibuprofen, 13107-004 — Hydrocodone Bitartrate and Ibuprofen, 17856-5309 — Ibuprofen, 21130-006 — Ibuprofen, 21130-032 — Ibuprofen, 21130-056 — Diphenhydramine Citrate, Ibuprofen, 21130-070 — Ibuprofen, 21130-216 — IBUPROFEN, 21130-220 — Ibuprofen, 21130-228 — Ibuprofen and Diphenhydramine Citrate, 21130-261 — Ibuprofen, 21130-358 — Ibuprofen, 21130-359 — 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.