PEG-3350 and Electrolytes
- Product NDC
- 10572-101
- 11-digit product format
- 105720101
- Labeler code
- 10572
- Product ID
- 10572-101_e9bdf1ea-2513-c298-e053-2a95a90a601e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Affordable Pharmaceuticals, LLC
- Application
- NDA019011
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2009-07-01
- Marketing end
- 2024-02-29
- Substance
- POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
- Active strength
- 236 g/4L; g/4L; g/4L; g/4L; g/4L
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], 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 Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10572-101-01 | PEG-3350 and Electrolytes | 4 L in 1 JUG | POWDER, FOR SOLUTION | 4 | 7 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 10572-101-01 | ML - Milliliter | 10572-101 | 8f1e1c31-d3ed-4bbb-b161-7b62703826ab | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10572-101 | PEG-3350 AND ELECTROLYTES (POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE) POWDER, FOR SOLUTION [AFFORDABLE PHARMACEUTICALS, LLC] | 7 | Legacy NDC, 1 package rows | 20220929_448db7a5-1fea-4bf3-b1f5-e9d027a36603.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 966920 | polyethylene glycol 3350 236 GM / potassium chloride 2.97 GM / sodium bicarbonate 6.74 GM / sodium chloride 5.86 GM / sodium sulfate 22.74 GM Powder for Oral Solution | PSN | 448db7a5-1fea-4bf3-b1f5-e9d027a36603 | 7 |
| 966920 | polyethylene glycol 3350 236000 MG / potassium chloride 2970 MG / sodium bicarbonate 6740 MG / sodium chloride 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution | SCD | 448db7a5-1fea-4bf3-b1f5-e9d027a36603 | 7 |
| 966920 | polyethylene glycol 3350 236 GM / potassium chloride 2.97 GM / sodium bicarbonate 6.74 GM / sodium chloride 5.86 GM / sodium sulfate 22.74 GM Powder for Oral Solution | SY | 448db7a5-1fea-4bf3-b1f5-e9d027a36603 | 7 |
| 966920 | POLYETHYLENE GLYCOL 3350 236000 MG / K+ Chloride 2970 MG / NaHCO3 6740 MG / NaCl 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution | SY | 448db7a5-1fea-4bf3-b1f5-e9d027a36603 | 7 |
| 966920 | POLYETHYLENE GLYCOL 3350 236000 MG / Pot Chloride 2970 MG / NaHCO3 6740 MG / NaCl 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution | SY | 448db7a5-1fea-4bf3-b1f5-e9d027a36603 | 7 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 10572-101-01 | 10572010101 | 4 L in 1 JUG (10572-101-01) | 4 l | 2009-07-01 | 0000-00-00 | No | No | Current |