NDC Product
Human Prescription DrugGralise NDC 52427-803
- Generic Name
- Gabapentin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
The following National Drug Codes (NDCs) are directly associated with the clinical concept for Gabapentin sample pack 300 mg (9), 600 mg (24) Once-Daily Oral Tablet (RxCUI 2398511). 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.