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United States · US · US:61755-056_d82c287f-a94e-4831-9991-4742cdd17348
LYNOZYFIC
UNIISPLATC L01FX
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRegeneron Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeL01FX
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1161755056011 VIAL, SINGLE-DOSE in 1 CARTON (61755-056-01) / 10 mL in 1 VIAL, SINGLE-DOSE (61755-056-00)
Annotations
UNII (FDA Substance ID)
M3CPC50MZS
LINVOSELTAMAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "M3CPC50MZS",
"rxcui": null,
"inchikey": null,
"display_name": "LINVOSELTAMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"e9fd0739-1b3f-4b8b-824a-1f0a902384d3": {
"match": "brand_token",
"title": "LYNOZYFIC (LINVOSELTAMAB-GCPT) INJECTION, SOLUTION, CONCENTRATE [REGENERON PHARMACEUTICALS, INC.]",
"spl_version": "6",
"published_date": "2025-07-16"
}
},
"productid": "61755-056_d82c287f-a94e-4831-9991-4742cdd17348",
"productndc": "61755-056",
"dosage_form": "INJECTION, SOLUTION, CONCENTRATE",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LINVOSELTAMAB",
"proprietary_name": "LYNOZYFIC",
"active_ingred_unit": "mg/10mL",
"application_number": "BLA761400",
"marketing_category": "BLA",
"nonproprietary_name": "linvoseltamab-gcpt",
"start_marketing_date": "20250702",
"active_numerator_strength": "200"
}Related drugs
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- ISLynozyficRegeneron Ireland Designated Activity Company
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