NDC Product
Human Prescription DrugFluoxetine Hydrochloride NDC 55111-284
- Generic Name
- Fluoxetine Hydrochloride
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
The following National Drug Codes (NDCs) are directly associated with the clinical concept for FLUoxetine 90 mg Delayed Release Oral Capsule (RxCUI 313995). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.
Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.