NDC 55566-1600 - Menopur
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 55566-1600
- Manufacturer
- Ferring Pharmaceuticals Inc.
- Effective date
- 2024-11-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Menopur - Ferring Pharmaceuticals Inc. | Ferring Pharmaceuticals Inc. | 2024-11-21 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55566-1600-0 | Menopur | 1 in 1 VIAL | INJECTION | 5 | 9 mg | 47 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Follitropin | ACTIVE INGREDIENT | 076WHW89TW | MENOPUR (FOLLITROPIN AND LUTEINIZING HORMONE) KIT [FERRING PHARMACEUTICALS INC.] | 13 | |
| Luteinizing Hormone | ACTIVE INGREDIENT | 8XA4VN1LH4 | MENOPUR (FOLLITROPIN AND LUTEINIZING HORMONE) KIT [FERRING PHARMACEUTICALS INC.] | 13 | |
| Follitropin | ACTIVE MOIETY | 076WHW89TW | MENOPUR (FOLLITROPIN AND LUTEINIZING HORMONE) KIT [FERRING PHARMACEUTICALS INC.] | 13 | |
| Luteinizing Hormone | ACTIVE MOIETY | 8XA4VN1LH4 | MENOPUR (FOLLITROPIN AND LUTEINIZING HORMONE) KIT [FERRING PHARMACEUTICALS INC.] | 13 | |
| Lactose Monohydrate | INACTIVE INGREDIENT | EWQ57Q8I5X | MENOPUR (FOLLITROPIN AND LUTEINIZING HORMONE) KIT [FERRING PHARMACEUTICALS INC.] | 13 | |
| Polysorbate 20 | INACTIVE INGREDIENT | 7T1F30V5YH | MENOPUR (FOLLITROPIN AND LUTEINIZING HORMONE) KIT [FERRING PHARMACEUTICALS INC.] | 13 | |
| Sodium Phosphate, Dibasic, Heptahydrate | INACTIVE INGREDIENT | 70WT22SF4B | MENOPUR (FOLLITROPIN AND LUTEINIZING HORMONE) KIT [FERRING PHARMACEUTICALS INC.] | 13 |