NDC Product
Human Prescription DrugDexlansoprazole NDC 50090-7451
- Generic Name
- Dexlansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
This profile provides standardized clinical and technical data for Lauryl Sulfate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) DIQ16UC154.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 151-41-7 and the RxNorm Concept ID (RxCUI) 1362927. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C12H26O4S MOTZDAYCYVMXPC-UHFFFAOYSA-N This section provides a complete list of nomenclature and identifier mappings for Lauryl Sulfate. 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: