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Luveris
Luveris - 44087-1375-1 - (lutropin alfa)
Drug Information of Luveris
| Product NDC: | 44087-1375 |
| Proprietary Name: | Luveris |
| Non Proprietary Name: | lutropin alfa |
| Active Ingredient(s): | & nbsp; lutropin alfa |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Luveris
| Product NDC: | 44087-1375 |
| Labeler Name: | EMD Serono, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021322 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20041008 |
Package Information of Luveris
| Package NDC: | 44087-1375-1 |
| Package Description: | 1 KIT in 1 CARTON (44087-1375-1) * 1 mL in 1 VIAL * 1 mL in 1 VIAL (44087-9999-1) |
NDC Information of Luveris
| NDC Code | 44087-1375-1 |
| Proprietary Name | Luveris |
| Package Description | 1 KIT in 1 CARTON (44087-1375-1) * 1 mL in 1 VIAL * 1 mL in 1 VIAL (44087-9999-1) |
| Product NDC | 44087-1375 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lutropin alfa |
| Dosage Form Name | KIT |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20041008 |
| Marketing Category Name | NDA |
| Labeler Name | EMD Serono, Inc. |
| Substance Name | |
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