NDC 66658-501

GAMIFANT

(emapalumab-lzsg)

GAMIFANT is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Swedish Orphan Biovitrum Ab (publ). The primary component is Emapalumab.

Product ID66658-501_41ca7358-b40f-4721-a585-d9466faf8aa9
NDC66658-501
Product TypeHuman Prescription Drug
Proprietary NameGAMIFANT
Generic Name(emapalumab-lzsg)
Dosage FormInjection
Route of AdministrationINTRAVENOUS
Marketing Start Date2019-05-17
Marketing CategoryBLA / BLA
Application NumberBLA761107
Labeler NameSwedish Orphan Biovitrum AB (publ)
Substance NameEMAPALUMAB
Active Ingredient Strength10 mg/2mL
Pharm ClassesInterferon gamma Blocker [EPC],Interferon gamma Antagonists [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 66658-501-01

1 VIAL, SINGLE-USE in 1 CARTON (66658-501-01) > 2 mL in 1 VIAL, SINGLE-USE
Marketing Start Date2019-05-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66658-501-01 [66658050101]

GAMIFANT INJECTION
Marketing CategoryBLA
Application NumberBLA761107
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-17

Drug Details

Active Ingredients

IngredientStrength
EMAPALUMAB10 mg/2mL

OpenFDA Data

SPL SET ID:a865e0ef-8685-4f69-8838-648c4f3bab47
Manufacturer
UNII

Pharmacological Class

  • Interferon gamma Blocker [EPC]
  • Interferon gamma Antagonists [MoA]

NDC Crossover Matching brand name "GAMIFANT" or generic name "(emapalumab-lzsg)"

NDCBrand NameGeneric Name
66658-501GAMIFANT(emapalumab-lzsg)
66658-505GAMIFANT(emapalumab-lzsg)
66658-510GAMIFANT(emapalumab-lzsg)
72171-501GAMIFANT(emapalumab-lzsg)
72171-505GAMIFANT(emapalumab-lzsg)

Trademark Results [GAMIFANT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
GAMIFANT
GAMIFANT
87283834 5505933 Live/Registered
EMACO SA
2016-12-29

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