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GoLYTELY
GoLYTELY - 52268-700-01 - (POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, Sodium CHLORIDE, POTASSIUM CHLORIDE)
Drug Information of GoLYTELY
| Product NDC: | 52268-700 |
| Proprietary Name: | GoLYTELY |
| Non Proprietary Name: | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, Sodium CHLORIDE, POTASSIUM CHLORIDE |
| Active Ingredient(s): | 60; .745; 1.68; 1.46; 5.86 g/L; g/L; g/L; g/L; g/L & nbsp; POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, Sodium CHLORIDE, POTASSIUM CHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GoLYTELY
| Product NDC: | 52268-700 |
| Labeler Name: | Braintree Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019011 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19840713 |
Package Information of GoLYTELY
| Package NDC: | 52268-700-01 |
| Package Description: | 3.785 L in 1 PACKET (52268-700-01) |
NDC Information of GoLYTELY
| NDC Code | 52268-700-01 |
| Proprietary Name | GoLYTELY |
| Package Description | 3.785 L in 1 PACKET (52268-700-01) |
| Product NDC | 52268-700 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, Sodium CHLORIDE, POTASSIUM CHLORIDE |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 19840713 |
| Marketing Category Name | NDA |
| Labeler Name | Braintree Laboratories, Inc. |
| Substance Name | POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS |
| Strength Number | 60; .745; 1.68; 1.46; 5.86 |
| Strength Unit | g/L; g/L; g/L; g/L; g/L |
| Pharmaceutical Classes | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
