Product NDC: | 35356-544 |
Proprietary Name: | Polyethylene Glycol 3350 |
Non Proprietary Name: | Polyethylene Glycol 3350 |
Active Ingredient(s): | 17 g/17g & nbsp; Polyethylene Glycol 3350 |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-544 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077706 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060906 |
Package NDC: | 35356-544-01 |
Package Description: | 527 g in 1 BOTTLE (35356-544-01) |
NDC Code | 35356-544-01 |
Proprietary Name | Polyethylene Glycol 3350 |
Package Description | 527 g in 1 BOTTLE (35356-544-01) |
Product NDC | 35356-544 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Polyethylene Glycol 3350 |
Dosage Form Name | POWDER, FOR SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20060906 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | POLYETHYLENE GLYCOL 3350 |
Strength Number | 17 |
Strength Unit | g/17g |
Pharmaceutical Classes | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |