Chlorpheniramine maleate; ibuprofen; phenylephrine hydrochloride
Chlorpheniramine maleate; ibuprofen; phenylephrine hydrochloride: 1 brand, 0 generics; first approved Dec 21, 2011.
No listed patents or exclusivity: brand product(s) only.
Brand (NDA) products
- HALEON US HOLDINGSNDA 02211320112 strengths
Approved strengths under this FDA application. Strength Dosage form Route Status TE 4MG;200MG;10MG TABLET ORAL OTC — 4MG;200MG;10MG TABLET ORAL OTC —
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
Approval history
Approvals span 2011–2017 across 1 FDA application.
Chlorpheniramine maleate; ibuprofen; phenylephrine hydrochloride: frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.
Built directly from the FDA Orange Book data file (products, patents, and exclusivity). TE codes, RLD/RS flags, patent expirations, and exclusivity dates match the official FDA record. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
Related FDA reference tools
- FDA Purple BookLicensed biologics, biosimilars, interchangeables, BLA records, and exclusivity dates.
- FDA BiosimilarsFDA-approved biosimilars and interchangeable biosimilars, by reference product.
- 510(k) Predicate DatabaseSearch FDA 510(k) clearances and map predicate-device lineage.
- FDA 483 DatabaseFDA Form 483 observations and inspection records by firm, date, and citation.
