NDC Product
Human Otc DrugDramamine NDC 63029-913
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
This profile provides standardized clinical and technical data for Meclizine Monohydrochloride Anhydrous, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 008PUV3986.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 410538-37-3 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.
C25H27ClN2.ClH GJNMJOHYRWHJQB-UHFFFAOYSA-N This section provides a complete list of nomenclature and identifier mappings for Meclizine Monohydrochloride Anhydrous. 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: