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Panretin
Panretin - 62856-601-22 - (alitretinoin)
Drug Information of Panretin
| Product NDC: | 62856-601 |
| Proprietary Name: | Panretin |
| Non Proprietary Name: | alitretinoin |
| Active Ingredient(s): | 60 mg/60g & nbsp; alitretinoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Panretin
| Product NDC: | 62856-601 |
| Labeler Name: | Eisai Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020886 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19990203 |
Package Information of Panretin
| Package NDC: | 62856-601-22 |
| Package Description: | 60 g in 1 TUBE (62856-601-22) |
NDC Information of Panretin
| NDC Code | 62856-601-22 |
| Proprietary Name | Panretin |
| Package Description | 60 g in 1 TUBE (62856-601-22) |
| Product NDC | 62856-601 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alitretinoin |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19990203 |
| Marketing Category Name | NDA |
| Labeler Name | Eisai Inc. |
| Substance Name | ALITRETINOIN |
| Strength Number | 60 |
| Strength Unit | mg/60g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
