United States · FDA National Drug Code directory

CHILDRENS Ibuprofen

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
81033-019_4f5ac0eb-734b-1e32-e063-6294a90a9f82
Product NDC
81033-019
Form
SUSPENSION
Composition / generic term
Ibuprofen
Labeler
Kesin Pharma Corporation
Marketing category
ANDA
Marketing start / end (source format)
20110428
Source listing expiry
20271231

Source-listed ingredients

  • IBUPROFEN — 100 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CUP, UNIT-DOSE in 1 CASE (81033-019-01) / 5 mL in 1 CUP, UNIT-DOSE (81033-019-05) · 81033-019-01
  • 100 CUP, UNIT-DOSE in 1 CASE (81033-019-02) / 10 mL in 1 CUP, UNIT-DOSE (81033-019-10) · 81033-019-02

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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