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IBUPROFEN

NDC 60760-604 · St. Mary's Medical Park Pharmacy

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

60760-604-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59779-685 — Ibuprofen, 59779-897 — Ibuprofen, 59779-971 — Ibuprofen, 60687-446 — Ibuprofen, 60687-457 — Ibuprofen, 60687-468 — Ibuprofen, 60687-743 — Ibuprofen, 60760-596 — Ibuprofen, 60760-597 — Ibuprofen, 60760-603 — IBUPROFEN, 60760-844 — Ibuprofen, 60760-929 — Ibuprofen, 61245-084 — Ibuprofen, 61245-085 — Ibuprofen, 61504-109 — Ibuprofen, 61504-110 — Ibuprofen, 61504-185 — Ibuprofen, 61919-463 — IBUOROFEN, 62011-0070 — Ibuprofen and Pseudoephedrine Hydrochloride, 62011-0368 — 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.

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