NDC 51672-4170 – Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit
Sodium Sulfate Anhydrous 17.5 g/177mL; Potassium Sulfate 3.13 g/177mL; Magnesium Sulfate, Unspecified Form 1.6 g/177mL · Solution · Oral
Product NDC51672-4170
Product details
- Brand name
- Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit
- Generic name
- Sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA206431
- Marketed since
- March 27, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Calculi Dissolution Agent; Osmotic Laxative; Osmotic Laxative
Active ingredients
- Sodium Sulfate Anhydrous 17.5 g/177mL
- Potassium Sulfate 3.13 g/177mL
- Magnesium Sulfate, Unspecified Form 1.6 g/177mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4170-5 | 2 BOTTLE in 1 CARTON (51672-4170-5) / 177 mL in 1 BOTTLE | Mar 27, 2024 |