Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate
- Product NDC
- 67877-725
- 11-digit product format
- 678770725
- Labeler code
- 67877
- Product ID
- 67877-725_a55745d9-2b54-474d-9250-0447cbee6668
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Ascend Laboratories, LLC
- Application
- ANDA213924
- Marketing category
- ANDA
- Marketing start
- 2024-03-29
- Substance
- MAGNESIUM SULFATE, UNSPECIFIED FORM; POTASSIUM SULFATE; SODIUM SULFATE
- Active strength
- 1.6; 3.13; 17.5 g/177mL; g/177mL; g/177mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], 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 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 Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM SULFATE | 1.6 g/177mL |
| POTASSIUM SULFATE | 3.13 g/177mL |
| MAGNESIUM SULFATE, UNSPECIFIED FORM | 17.5 g/177mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0YPR65R21J, 1K573LC5TV, DE08037SAB |
| Rxcui | 1120068 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67877-725-92 | Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate | 2 in 1 CARTON | SOLUTION | 2 | | 5 |
| 67877-725-92 | Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate | 177 mL in 1 BOTTLE, PLASTIC | SOLUTION | 177 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67877-725 | SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE SOLUTION [ASCEND LABORATORIES, LLC] | 5 | Current NDC, 2 package rows | 20240331_2106d1aa-086e-4248-9a3d-ec138d492cf3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 67877-725-92 | 67877072592 | 2 BOTTLE, PLASTIC in 1 CARTON (67877-725-92) / 177 mL in 1 BOTTLE, PLASTIC | 2024-03-29 | No | No | Historical |