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Ibuprofen

NDC 76420-846 · Asclemed USA, Inc.

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength400 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

76420-846-01 — 100 TABLET, FILM COATED in 1 BOTTLE (76420-846-01)

76420-846-05 — 500 TABLET, FILM COATED in 1 BOTTLE (76420-846-05)

76420-846-30 — 30 TABLET, FILM COATED in 1 BOTTLE (76420-846-30)

76420-846-60 — 60 TABLET, FILM COATED in 1 BOTTLE (76420-846-60)

76420-846-90 — 90 TABLET, FILM COATED in 1 BOTTLE (76420-846-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76281-119 — IBUPROFEN, 76281-126 — IBUPROFEN, 76281-128 — IBUPROFEN, 76282-712 — Ibuprofen, 76282-713 — Ibuprofen, 76282-714 — Ibuprofen, 76420-415 — ibuprofen, 76420-575 — Ibuprofen, 76420-576 — Ibuprofen, 76420-577 — Ibuprofen, 76420-847 — Ibuprofen, 76420-848 — Ibuprofen, 76420-891 — Ibuprofen and famotidine, 79395-003 — Ibuprofen, 79481-0152 — acetaminophen, ibuprofen, 79481-0392 — Ibuprofen, 79481-0419 — ibuprofen, 79481-0423 — Ibuprofen, 79481-0503 — Acetaminophen, Ibuprofen, 79481-3000 — 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.