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Menopur
Menopur - 55566-7501-2 - (Follitropin and Luteinizing Hormone)
Drug Information of Menopur
| Product NDC: | 55566-7501 |
| Proprietary Name: | Menopur |
| Non Proprietary Name: | Follitropin and Luteinizing Hormone |
| Active Ingredient(s): | & nbsp; Follitropin and Luteinizing Hormone |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Menopur
| Product NDC: | 55566-7501 |
| Labeler Name: | Ferring Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021663 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20041029 |
Package Information of Menopur
| Package NDC: | 55566-7501-2 |
| Package Description: | 1 CARTON in 1 CARTON (55566-7501-2) > 1 KIT in 1 CARTON (55566-7501-1) * 2 mL in 1 VIAL (55566-7502-0) * 1 mL in 1 VIAL (0641-0495-17) |
NDC Information of Menopur
| NDC Code | 55566-7501-2 |
| Proprietary Name | Menopur |
| Package Description | 1 CARTON in 1 CARTON (55566-7501-2) > 1 KIT in 1 CARTON (55566-7501-1) * 2 mL in 1 VIAL (55566-7502-0) * 1 mL in 1 VIAL (0641-0495-17) |
| Product NDC | 55566-7501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Follitropin and Luteinizing Hormone |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20041029 |
| Marketing Category Name | NDA |
| Labeler Name | Ferring Pharmaceuticals Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
