NDC Product
Human Prescription DrugCefoxitin And Dextrose NDC 0264-3123
- Generic Name
- Cefoxitin Sodium
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
This profile provides standardized clinical and technical data for Cefoxitin Sodium, uniquely identified by the FDA Unique Ingredient Identifier (UNII) Q68050H03T.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 33564-30-6 and the RxNorm Concept ID (RxCUI) 203118. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C16H16N3O7S2.Na GNWUOVJNSFPWDD-XMZRARIVSA-M This section provides a complete list of nomenclature and identifier mappings for Cefoxitin Sodium. 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: