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Oxsoralen-Ultra
Oxsoralen-Ultra - 0187-0650-42 - (Methoxsalen)
Drug Information of Oxsoralen-Ultra
| Product NDC: | 0187-0650 |
| Proprietary Name: | Oxsoralen-Ultra |
| Non Proprietary Name: | Methoxsalen |
| Active Ingredient(s): | 10 mg/1 & nbsp; Methoxsalen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxsoralen-Ultra
| Product NDC: | 0187-0650 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019600 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19861030 |
Package Information of Oxsoralen-Ultra
| Package NDC: | 0187-0650-42 |
| Package Description: | 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, GLASS (0187-0650-42) |
NDC Information of Oxsoralen-Ultra
| NDC Code | 0187-0650-42 |
| Proprietary Name | Oxsoralen-Ultra |
| Package Description | 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, GLASS (0187-0650-42) |
| Product NDC | 0187-0650 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methoxsalen |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 19861030 |
| Marketing Category Name | NDA |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | METHOXSALEN |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Photoabsorption [MoA],Photoactivated Radical Generator [EPC],Photosensitizing Activity [PE],Psoralen [EPC],Psoralens [Chemical/Ingredient] |
