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TRILYTE
TRILYTE - 68220-131-04 - (Polyethylene Glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride)
Drug Information of TRILYTE
| Product NDC: | 68220-131 |
| Proprietary Name: | TRILYTE |
| Non Proprietary Name: | Polyethylene Glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Active Ingredient(s): | 420; 1.48; 5.72; 11.2 g/4L; g/4L; g/4L; g/4L & nbsp; Polyethylene Glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Administration Route(s): | NASOGASTRIC; ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRILYTE
| Product NDC: | 68220-131 |
| Labeler Name: | Alaven Pharmaceutical LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076491 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040624 |
Package Information of TRILYTE
| Package NDC: | 68220-131-04 |
| Package Description: | 4 L in 1 BOTTLE (68220-131-04) |
NDC Information of TRILYTE
| NDC Code | 68220-131-04 |
| Proprietary Name | TRILYTE |
| Package Description | 4 L in 1 BOTTLE (68220-131-04) |
| Product NDC | 68220-131 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Polyethylene Glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | NASOGASTRIC; ORAL |
| Start Marketing Date | 20040624 |
| Marketing Category Name | ANDA |
| Labeler Name | Alaven Pharmaceutical LLC |
| Substance Name | POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE |
| Strength Number | 420; 1.48; 5.72; 11.2 |
| Strength Unit | 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] |
