NDC Product
Human Otc DrugGaviscon NDC 0135-0094
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
The following National Drug Codes (NDCs) are directly associated with the clinical concept for Gaviscon Extra Strength 254 mg / 237.5 mg in 5 mL Oral Suspension (RxCUI 404472). 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.