Menopur
These highlights do not include all the information needed to use MENOPUR safely and effectively. See full prescribing information for MENOPUR. MENOPUR (menotropins for injection) for subcutaneous use. Initial U.S. Approval: 1975
Approved
Approval ID
22c8db95-c3db-1770-8086-31356fbabe35
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 7, 2021
Manufacturers
FDA
Ferring Pharmaceuticals Inc.
DUNS: 103722955
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
menotropins
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code55566-7501
Application NumberBLA021663
Product Classification
M
Marketing Category
C73585
G
Generic Name
menotropins
Product Specifications
Effective DateMay 1, 2018
FDA Product Classification