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up and up powderlax
up and up powderlax - 11673-306-03 - (Polyethylene Glycol 3350)
Drug Information of up and up powderlax
| Product NDC: | 11673-306 |
| Proprietary Name: | up and up powderlax |
| 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 up and up powderlax
| Product NDC: | 11673-306 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090685 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091007 |
Package Information of up and up powderlax
| Package NDC: | 11673-306-03 |
| Package Description: | 510 g in 1 BOTTLE (11673-306-03) |
NDC Information of up and up powderlax
| NDC Code | 11673-306-03 |
| Proprietary Name | up and up powderlax |
| Package Description | 510 g in 1 BOTTLE (11673-306-03) |
| Product NDC | 11673-306 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polyethylene Glycol 3350 |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091007 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Corporation |
| Substance Name | POLYETHYLENE GLYCOL 3350 |
| Strength Number | 17 |
| Strength Unit | g/17g |
| Pharmaceutical Classes |
