Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit
NDC 51672-4170, sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate, solution, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 51672-4170
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206431
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4170 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM SULFATE ANHYDROUS17.5 g/177mL
- POTASSIUM SULFATE3.13 g/177mL
- MAGNESIUM SULFATE, UNSPECIFIED FORM1.6 g/177mL
Pharmacologic classes
Calculi Dissolution Agent [EPC]; Increased Large Intestinal Motility [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51672-4170-5 | 51672417005 | 2 BOTTLE in 1 CARTON (51672-4170-5) / 177 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/4adeeb11-0f3a-47d8-a664-376df50b05f2NADAC price for package 51672417005
GET /v1/drugs/nadac/51672417005
Use it
Look up 51672-4170 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4170 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51672-4170. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.