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Polyethylene Glycol 3350
Polyethylene Glycol 3350 - 0722-6920-01 - (Polyethylene Glycol 3350)
Drug Information of Polyethylene Glycol 3350
| Product NDC: | 0722-6920 |
| Proprietary Name: | Polyethylene Glycol 3350 |
| Non Proprietary Name: | Polyethylene Glycol 3350 |
| Active Ingredient(s): | 17 g/1 & nbsp; Polyethylene Glycol 3350 |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Polyethylene Glycol 3350
| Product NDC: | 0722-6920 |
| Labeler Name: | Nexgen Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077706 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060927 |
Package Information of Polyethylene Glycol 3350
| Package NDC: | 0722-6920-01 |
| Package Description: | 255 POWDER, FOR SOLUTION in 1 BOTTLE, PLASTIC (0722-6920-01) |
NDC Information of Polyethylene Glycol 3350
| NDC Code | 0722-6920-01 |
| Proprietary Name | Polyethylene Glycol 3350 |
| Package Description | 255 POWDER, FOR SOLUTION in 1 BOTTLE, PLASTIC (0722-6920-01) |
| Product NDC | 0722-6920 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Polyethylene Glycol 3350 |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20060927 |
| Marketing Category Name | ANDA |
| Labeler Name | Nexgen Pharma, Inc. |
| Substance Name | POLYETHYLENE GLYCOL 3350 |
| Strength Number | 17 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
