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Clenz-Lyte
Clenz-Lyte - 0574-0427-04 - (Polyethylene Glycol 3350)
Drug Information of Clenz-Lyte
| Product NDC: | 0574-0427 |
| Proprietary Name: | Clenz-Lyte |
| Non Proprietary Name: | Polyethylene Glycol 3350 |
| Active Ingredient(s): | 236; 2.97; 6.74; 5.86; 22.74 g/4L; g/4L; g/4L; g/4L; g/4L & nbsp; Polyethylene Glycol 3350 |
| Administration Route(s): | NASOGASTRIC; ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clenz-Lyte
| Product NDC: | 0574-0427 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090769 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100607 |
Package Information of Clenz-Lyte
| Package NDC: | 0574-0427-04 |
| Package Description: | 4 L in 1 JUG (0574-0427-04) |
NDC Information of Clenz-Lyte
| NDC Code | 0574-0427-04 |
| Proprietary Name | Clenz-Lyte |
| Package Description | 4 L in 1 JUG (0574-0427-04) |
| Product NDC | 0574-0427 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Polyethylene Glycol 3350 |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | NASOGASTRIC; ORAL |
| Start Marketing Date | 20100607 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS |
| Strength Number | 236; 2.97; 6.74; 5.86; 22.74 |
| Strength Unit | g/4L; g/4L; g/4L; g/4L; g/4L |
| Pharmaceutical Classes | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
