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Targretin
Targretin - 62856-604-22 - (bexarotene)
Drug Information of Targretin
| Product NDC: | 62856-604 |
| Proprietary Name: | Targretin |
| Non Proprietary Name: | bexarotene |
| Active Ingredient(s): | 1 g/100g & nbsp; bexarotene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Targretin
| Product NDC: | 62856-604 |
| Labeler Name: | Eisai Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021056 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000628 |
Package Information of Targretin
| Package NDC: | 62856-604-22 |
| Package Description: | 60 g in 1 TUBE (62856-604-22) |
NDC Information of Targretin
| NDC Code | 62856-604-22 |
| Proprietary Name | Targretin |
| Package Description | 60 g in 1 TUBE (62856-604-22) |
| Product NDC | 62856-604 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bexarotene |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20000628 |
| Marketing Category Name | NDA |
| Labeler Name | Eisai Inc. |
| Substance Name | BEXAROTENE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
