NDC Product
Standardized AllergenicT.r.u.e. Test Thin-layer Rapid Use Patch Test NDC 67334-0457
- Generic Name
- Standardized Allergenic
- Dosage Form
- Kit
- Route
- Cutaneous
- Marketing
- BLA
Active Listing
This profile provides standardized clinical and technical data for Tixocortol, uniquely identified by the FDA Unique Ingredient Identifier (UNII) ZX3KEK657Z.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 61951-99-3 and the RxNorm Concept ID (RxCUI) 57257. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C21H30O4S YWDBSCORAARPPF-VWUMJDOOSA-N This section provides a complete list of nomenclature and identifier mappings for Tixocortol. 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: