follicle stimulating hormone 75 UNT / luteinizing hormone 75 UNT Injection

RxCUI
314097
RxNorm name
follicle stimulating hormone 75 UNT / luteinizing hormone 75 UNT Injection
Display name
follicle stimulating hormone 75 UNT / luteinizing hormone 75 UNT Injection
Full name
follicle stimulating hormone 75 UNT / luteinizing hormone 75 UNT Injection
Term type
SCD
Status
DailyMed mapping
Updated
2026-06-04 23:38:50

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
021663Menopurmenotropins351(a)Rx2026-07-01

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MenopurMENOTROPINSFerring Pharmaceuticals Inc.22c8db95-c3db-1770-8086-31356fbabe352018-05-31Warnings, Adverse reactionsExact identifier
rxcui: 314097

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
22c8db95-c3db-1770-8086-31356fbabe35menotropins 75 UNT Injection [PSN] · follicle stimulating hormone 75 UNT / luteinizing hormone 75 UNT Injection [SCD] · FSH 75 UNT / LH 75 UNT Injection [SY] · menotropins (FSH) 75 UNT / menotropins (LH) 75 UNT Injection [SY] · menotropins 75 UNT Injection [SY]547These 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: 197520180531