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Hexalen
Hexalen - 62856-001-10 - (altretamine)
Drug Information of Hexalen
| Product NDC: | 62856-001 |
| Proprietary Name: | Hexalen |
| Non Proprietary Name: | altretamine |
| Active Ingredient(s): | 50 mg/1 & nbsp; altretamine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hexalen
| Product NDC: | 62856-001 |
| Labeler Name: | Eisai Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019926 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19901226 |
Package Information of Hexalen
| Package NDC: | 62856-001-10 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (62856-001-10) |
NDC Information of Hexalen
| NDC Code | 62856-001-10 |
| Proprietary Name | Hexalen |
| Package Description | 100 CAPSULE in 1 BOTTLE (62856-001-10) |
| Product NDC | 62856-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | altretamine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19901226 |
| Marketing Category Name | NDA |
| Labeler Name | Eisai Inc. |
| Substance Name | ALTRETAMINE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
