NDC Product
Human Prescription DrugAcebutolol Hydrochloride NDC 62559-255
- Generic Name
- Acebutolol Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
This profile provides standardized clinical and technical data for Acebutolol, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 67P356D8GH.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 37517-30-9 and the RxNorm Concept ID (RxCUI) 149. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C18H28N2O4 GOEMGAFJFRBGGG-UHFFFAOYSA-N This section provides a complete list of nomenclature and identifier mappings for Acebutolol. 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: