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Ibuprofen

NDC 70010-067 · Granules Pharmaceuticals Inc.

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

70010-067-01 — 100 TABLET, FILM COATED in 1 BOTTLE (70010-067-01)

70010-067-03 — 30 TABLET, FILM COATED in 1 BOTTLE (70010-067-03)

70010-067-05 — 500 TABLET, FILM COATED in 1 BOTTLE (70010-067-05)

70010-067-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (70010-067-10)

70010-067-50 — 50 TABLET, FILM COATED in 1 BOTTLE (70010-067-50)

70010-067-81 — 6 BLISTER PACK in 1 CARTON (70010-067-81) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70000-0263 — Ibuprofen, 70000-0264 — Ibuprofen, 70000-0291 — Ibuprofen, 70000-0298 — Ibuprofen, 70000-0571 — Ibuprofen, 70000-0597 — Ibuprofen, 70000-0606 — Ibuprofen and Pseudoephedrine HCl, 70000-0622 — Acetaminophen and Ibuprofen, 70000-0737 — Acetaminophen, Ibuprofen, 70010-066 — Ibuprofen, 70010-068 — Ibuprofen, 70010-131 — Acetaminophen and Ibuprofen, 70010-213 — Acetaminophen and Ibuprofen, 70038-131 — Acetaminophen, 70264-029 — IBUPROFEN, 70264-040 — Acetaminophen 250 mg and Ibuprofen 125 mg, 70264-041 — Ibuprofen, 70264-042 — Ibuprofen, 70264-043 — Ibuprofen, 70264-044 — 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.