SUPREP BOWEL PREP KIT
RxNorm 1001690 NDC Crossover

NDC Directory Crossover & Product Mapping

The following National Drug Codes (NDCs) are directly associated with the clinical concept for SUPREP BOWEL PREP KIT (RxCUI 1001690). 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.

Manufacturer Quick Index

→ Azurity Pharmaceuticals, Inc. 2
→ Braintree Laboratories, Inc. 2

Azurity Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Suprep Bowel Prep
NDC 24338-175

Generic Name
Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
Dosage Form
Solution, Concentrate
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Suprep Bowel Prep
NDC 24338-177

Generic Name
Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
Dosage Form
Solution, Concentrate
Route
Oral
Marketing
NDA
Active Listing

Braintree Laboratories, Inc.

NDC Product
Human Prescription Drug

Suprep Bowel Prep
NDC 52268-012

Generic Name
Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
Dosage Form
Solution, Concentrate
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Suprep Bowel Prep
NDC 52268-112

Generic Name
Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
Dosage Form
Solution, Concentrate
Route
Oral
Marketing
NDA
Active Listing