Skip to main content

Ibuprofen

NDC 51655-385 · Northwind Health Company, LLC

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength800 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

51655-385-26 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-26)

51655-385-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-932 — Ibuprofen, 51316-955 — Acetaminophen and Ibuprofen, 51407-369 — Ibuprofen, 51407-839 — Ibuprofen, 51407-840 — Ibuprofen, 51407-841 — Ibuprofen, 51655-042 — Ibuprofen, 51655-048 — Ibuprofen, 51655-275 — Ibuprofen, 51655-354 — ibuprofen, 51655-474 — Ibuprofen, 51655-757 — Ibuprofen, 51655-759 — Ibuprofen, 51660-423 — ibuprofen and pseudoephedrine hydrochloride, 51660-490 — Ibuprofen and Pseudoephedrine Hydrochloride, 51662-1582 — IBUPROFEN, 51672-1385 — Ibuprofen, 51672-1409 — Ibuprofen, 51672-2130 — Ibuprofen, 51672-2144 — 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.