Product NDC: | 54868-5160 |
Proprietary Name: | POLYETHYLENE GLYCOL 3350 |
Non Proprietary Name: | POLYETHYLENE GLYCOL 3350 |
Active Ingredient(s): | 1 g/g & nbsp; POLYETHYLENE GLYCOL 3350 |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5160 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076652 |
Marketing Category: | ANDA |
Start Marketing Date: | 20041007 |
Package NDC: | 54868-5160-1 |
Package Description: | 255 g in 1 BOTTLE (54868-5160-1) |
NDC Code | 54868-5160-1 |
Proprietary Name | POLYETHYLENE GLYCOL 3350 |
Package Description | 255 g in 1 BOTTLE (54868-5160-1) |
Product NDC | 54868-5160 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | POLYETHYLENE GLYCOL 3350 |
Dosage Form Name | POWDER |
Route Name | ORAL |
Start Marketing Date | 20041007 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | POLYETHYLENE GLYCOL 3350 |
Strength Number | 1 |
Strength Unit | g/g |
Pharmaceutical Classes | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |