NDC Product
Human Otc DrugCuprum Fluoratum NDC 37662-0949
- Generic Name
- Cuprum Fluoratum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
This profile provides standardized clinical and technical data for Cupric Fluoride Dihydrate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 3A38PC42E9.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 13454-88-1 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.
Cu.2F.2H2O CTRICEWDSISGPV-UHFFFAOYSA-L This section provides a complete list of nomenclature and identifier mappings for Cupric Fluoride Dihydrate. 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: