NDC Product
Human Prescription DrugKodatef NDC 71475-258
- Generic Name
- Tafenoquine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Inactive / Discontinued
This profile provides standardized clinical and technical data for Tafenoquine, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 262P8GS9L9.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 106635-80-7 and the RxNorm Concept ID (RxCUI) 2054023. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C24H28F3N3O3 LBHLFPGPEGDCJG-UHFFFAOYSA-N This section provides a complete list of nomenclature and identifier mappings for Tafenoquine. 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: