NDC Product
Human Prescription DrugProtopam Chloride NDC 60977-141
- Generic Name
- Pralidoxime Chloride
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intramuscular; Intravenous; Subcutaneous
- Marketing
- NDA
Active Listing
This profile provides standardized clinical and technical data for Pralidoxime, uniquely identified by the FDA Unique Ingredient Identifier (UNII) P7MU9UTP52.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25615-00-3 and the RxNorm Concept ID (RxCUI) 1546365. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C7H9N2O JBKPUQTUERUYQE-UHFFFAOYSA-O This section provides a complete list of nomenclature and identifier mappings for Pralidoxime. 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: