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Ibuprofen

NDC 21130-006 · BETTER LIVING BRANDS, LLC

Generic nameIbuprofen
Dosage formTABLET
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

21130-006-01 — 1 BOTTLE in 1 CARTON (21130-006-01) / 100 TABLET in 1 BOTTLE

21130-006-05 — 1 BOTTLE in 1 CARTON (21130-006-05) / 50 TABLET in 1 BOTTLE

21130-006-42 — 1 BOTTLE in 1 CARTON (21130-006-42) / 24 TABLET in 1 BOTTLE

21130-006-53 — 500 TABLET in 1 BOTTLE (21130-006-53)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 17856-5310 — 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, 21130-361 — 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.