| Product NDC: | 62175-442 |
| Proprietary Name: | POLYETHYLENE GLYCOL 3350 |
| Non Proprietary Name: | POLYETHYLENE GLYCOL 3350 |
| Active Ingredient(s): | 1 g/g & nbsp; POLYETHYLENE GLYCOL 3350 |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62175-442 |
| Labeler Name: | Kremers Urban Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076652 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111001 |
| Package NDC: | 62175-442-31 |
| Package Description: | 527 g in 1 BOTTLE (62175-442-31) |
| NDC Code | 62175-442-31 |
| Proprietary Name | POLYETHYLENE GLYCOL 3350 |
| Package Description | 527 g in 1 BOTTLE (62175-442-31) |
| Product NDC | 62175-442 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POLYETHYLENE GLYCOL 3350 |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20111001 |
| Marketing Category Name | ANDA |
| Labeler Name | Kremers Urban Pharmaceuticals Inc. |
| Substance Name | POLYETHYLENE GLYCOL 3350 |
| Strength Number | 1 |
| Strength Unit | g/g |
| Pharmaceutical Classes | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |