NDC Product
Human Prescription DrugOtezla NDC 55513-137
- Generic Name
- Apremilast
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
This profile provides standardized clinical and technical data for Apremilast, uniquely identified by the FDA Unique Ingredient Identifier (UNII) UP7QBP99PN.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 608141-41-9 and the RxNorm Concept ID (RxCUI) 1492727. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C22H24N2O7S IMOZEMNVLZVGJZ-QGZVFWFLSA-N This section provides a complete list of nomenclature and identifier mappings for Apremilast. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory: