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GlycoLax
GlycoLax - 62175-190-14 - (Polyethylene Glycol 3350)
Drug Information of GlycoLax
| Product NDC: | 62175-190 |
| Proprietary Name: | GlycoLax |
| 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 GlycoLax
| Product NDC: | 62175-190 |
| Labeler Name: | Kremers Urban Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090600 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091006 |
Package Information of GlycoLax
| Package NDC: | 62175-190-14 |
| Package Description: | 238 g in 1 BOTTLE (62175-190-14) |
NDC Information of GlycoLax
| NDC Code | 62175-190-14 |
| Proprietary Name | GlycoLax |
| Package Description | 238 g in 1 BOTTLE (62175-190-14) |
| Product NDC | 62175-190 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polyethylene Glycol 3350 |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20091006 |
| Marketing Category Name | ANDA |
| Labeler Name | Kremers Urban Pharmaceuticals Inc. |
| Substance Name | POLYETHYLENE GLYCOL 3350 |
| Strength Number | 17 |
| Strength Unit | g/17g |
| Pharmaceutical Classes |
