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Ibuprofen

NDC 71921-181 · Florida Pharmaceutical Products, LLC

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

71921-181-01 — 100 TABLET, FILM COATED in 1 BOTTLE (71921-181-01)

71921-181-50 — 500 TABLET, FILM COATED in 1 BOTTLE (71921-181-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-897 — Ibuprofen, 71610-898 — Ibuprofen, 71610-901 — Ibuprofen, 71610-902 — Ibuprofen, 71610-916 — Ibuprofen, 71610-967 — Ibuprofen, 71610-968 — Ibuprofen, 71610-969 — Ibuprofen, 71679-111 — Ibuprofen, 71921-180 — Ibuprofen, 71921-182 — Ibuprofen, 72036-015 — Ibuprofen, 72036-109 — Ibuprofen, 72036-110 — Ibuprofen, 72036-185 — Ibuprofen, 72036-211 — Ibuprofen, 72036-212 — Ibuprofen, 72090-070 — Ibuprofen, 72090-071 — Ibuprofen, 72162-1909 — Ibuprofen Oral, +1311 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels