NDC Product
Human Prescription DrugPrednisolone Sodium Phosphate NDC 50090-1582
- Generic Name
- Prednisolone Sodium Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
This profile provides standardized clinical and technical data for Dibasic Potassium Phosphate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) CI71S98N1Z.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 7758-11-4 and the RxNorm Concept ID (RxCUI) 55018. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
2K.HO4P ZPWVASYFFYYZEW-UHFFFAOYSA-L This section provides a complete list of nomenclature and identifier mappings for Dibasic Potassium Phosphate. 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: