| Product NDC: | 21695-598 |
| Proprietary Name: | Polyethylene Glycol 3350, NF Powder for Solution, Laxative |
| Non Proprietary Name: | Polyethylene Glycol 3350, NF Powder for Solution, Laxative |
| Active Ingredient(s): | 17 g/g & nbsp; Polyethylene Glycol 3350, NF Powder for Solution, Laxative |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 21695-598 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090812 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091007 |
| Package NDC: | 21695-598-25 |
| Package Description: | 255 g in 1 BOTTLE (21695-598-25) |
| NDC Code | 21695-598-25 |
| Proprietary Name | Polyethylene Glycol 3350, NF Powder for Solution, Laxative |
| Package Description | 255 g in 1 BOTTLE (21695-598-25) |
| Product NDC | 21695-598 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polyethylene Glycol 3350, NF Powder for Solution, Laxative |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091007 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | POLYETHYLENE GLYCOL 3350 |
| Strength Number | 17 |
| Strength Unit | g/g |
| Pharmaceutical Classes |