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Ibuprofen

NDC 37808-922 · H E B

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
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

37808-922-13 — 1 BOTTLE, PLASTIC in 1 CARTON (37808-922-13) / 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37808-363 — Ibuprofen, 37808-393 — Ibuprofen, 37808-410 — Ibuprofen, 37808-604 — Ibuprofen, 37808-609 — Ibuprofen, 37808-647 — Ibuprofen, 37808-699 — Ibuprofen, 37808-703 — diphenhydramine citrate, ibuprofen, 37808-709 — Ibuprofen, 37808-921 — Ibuprofen, 37835-581 — Ibuprofen, 37835-585 — Ibuprofen, 37835-588 — Ibuprofen, 41163-050 — diphenhydramine citrate, ibuprofen, 41163-057 — ibuprofen, 41163-103 — Acetaminophen, Ibuprofen, 41163-116 — Ibuprofen, 41163-158 — Ibuprofen, phenylephrine HCl, 41163-166 — Ibuprofen, 41163-185 — 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