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Childrens Ibuprofen Oral Suspension

NDC 0121-1666 · PAI Holdings, LLC dba PAI Pharma

Generic nameIbuprofen
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)IBUPROFEN
Strength200 mg/10mL
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

0121-1666-00 — 10 TRAY in 1 CASE (0121-1666-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1666-10)

0121-1666-40 — 4 TRAY in 1 CASE (0121-1666-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1666-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0113-1212 — Ibuprofen, 0113-2461 — Ibuprofen, 0113-4501 — ibuprofen, 0113-5299 — acetaminophen, ibuprofen, 0113-5300 — Acetaminophen, Ibuprofen, 0113-6040 — Ibuprofen, 0113-7366 — ibuprofen, 0121-0833 — Ibuprofen, 0121-0914 — Ibuprofen, 0121-1022 — Ibuprofen, 0121-1828 — Ibuprofen, 0121-2044 — Ibuprofen, 0143-9150 — acetaminophen and ibuprofen injection, 0143-9432 — ACETAMINOPHEN and IBUPROFEN, 0363-0050 — diphenhydramine citrate, ibuprofen, 0363-0103 — Ibuprofen, 0363-0166 — Ibuprofen, 0363-0207 — IBUPROFEN, DIPHENHYDRAMINE HCL, 0363-0221 — Ibuprofen, 0363-0222 — 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.