Product NDC: | 0722-7116 |
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/d & 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: | 0722-7116 |
Labeler Name: | Nexgen Pharma, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA090812 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091007 |
Package NDC: | 0722-7116-03 |
Package Description: | 30 d in 1 BOTTLE (0722-7116-03) |
NDC Code | 0722-7116-03 |
Proprietary Name | Polyethylene Glycol 3350, NF Powder for Solution, Laxative |
Package Description | 30 d in 1 BOTTLE (0722-7116-03) |
Product NDC | 0722-7116 |
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 | Nexgen Pharma, Inc. |
Substance Name | POLYETHYLENE GLYCOL 3350 |
Strength Number | 17 |
Strength Unit | g/d |
Pharmaceutical Classes |