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Polyethylene Glycol (3350)
Polyethylene Glycol (3350) - 51079-306-30 - (polyethylene glycol (3350))
Drug Information of Polyethylene Glycol (3350)
| Product NDC: | 51079-306 |
| 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) |
Labeler Information of Polyethylene Glycol (3350)
| Product NDC: | 51079-306 |
| Labeler Name: | UDL Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078915 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091120 |
Package Information of Polyethylene Glycol (3350)
| Package NDC: | 51079-306-30 |
| Package Description: | 30 POUCH in 1 CARTON (51079-306-30) > 17 g in 1 POUCH (51079-306-01) |
NDC Information of Polyethylene Glycol (3350)
| NDC Code | 51079-306-30 |
| Proprietary Name | Polyethylene Glycol (3350) |
| Package Description | 30 POUCH in 1 CARTON (51079-306-30) > 17 g in 1 POUCH (51079-306-01) |
| Product NDC | 51079-306 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | polyethylene glycol (3350) |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091120 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories Inc |
| Substance Name | POLYETHYLENE GLYCOL 3500 |
| Strength Number | 17 |
| Strength Unit | g/17g |
| Pharmaceutical Classes |
