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NuLYTELY
NuLYTELY - 52268-400-01 - (PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride)
Drug Information of NuLYTELY
| Product NDC: | 52268-400 |
| Proprietary Name: | NuLYTELY |
| Non Proprietary Name: | PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Active Ingredient(s): | 210; .74; 2.86; 5.6 g/2L; g/2L; g/2L; g/2L & nbsp; PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NuLYTELY
| Product NDC: | 52268-400 |
| Labeler Name: | Braintree Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019797 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070417 |
Package Information of NuLYTELY
| Package NDC: | 52268-400-01 |
| Package Description: | 4 L in 1 BOTTLE, PLASTIC (52268-400-01) |
NDC Information of NuLYTELY
| NDC Code | 52268-400-01 |
| Proprietary Name | NuLYTELY |
| Package Description | 4 L in 1 BOTTLE, PLASTIC (52268-400-01) |
| Product NDC | 52268-400 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20070417 |
| Marketing Category Name | NDA |
| Labeler Name | Braintree Laboratories, Inc. |
| Substance Name | POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE |
| Strength Number | 210; .74; 2.86; 5.6 |
| Strength Unit | g/2L; g/2L; g/2L; g/2L |
| Pharmaceutical Classes | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
