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Clearlax
Clearlax - 21695-566-10 - (polyethylene glycol)
Drug Information of Clearlax
| Product NDC: | 21695-566 |
| Proprietary Name: | Clearlax |
| Non Proprietary Name: | polyethylene glycol |
| Active Ingredient(s): | 17 g/1 & nbsp; polyethylene glycol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clearlax
| Product NDC: | 21695-566 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090685 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091007 |
Package Information of Clearlax
| Package NDC: | 21695-566-10 |
| Package Description: | 10 POWDER, FOR SOLUTION in 1 BOX (21695-566-10) |
NDC Information of Clearlax
| NDC Code | 21695-566-10 |
| Proprietary Name | Clearlax |
| Package Description | 10 POWDER, FOR SOLUTION in 1 BOX (21695-566-10) |
| Product NDC | 21695-566 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | polyethylene glycol |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091007 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | POLYETHYLENE GLYCOL 3350 |
| Strength Number | 17 |
| Strength Unit | g/1 |
| Pharmaceutical Classes |
