NDC Product
Human Prescription DrugOjjaara NDC 81864-101
- Generic Name
- Momelotinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
This profile provides standardized clinical and technical data for Momelotinib Dihydrochloride Monohydrate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) LDX8893L5D.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 1841094-17-4 and the RxNorm Concept ID (RxCUI) N/A. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C23H22N6O2.2ClH.H2O RQKCPSIFARJBOR-UHFFFAOYSA-N This section provides a complete list of nomenclature and identifier mappings for Momelotinib Dihydrochloride Monohydrate. 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: