NDC 54746-001

Alferon

Interferon Alfa-n3

Alferon is a Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by Hemispherx Biopharma, Inc. The primary component is Interferon Alfa-n3.

Product ID54746-001_77546126-9b82-08bd-e053-2991aa0a3b3d
NDC54746-001
Product TypeHuman Prescription Drug
Proprietary NameAlferon
Generic NameInterferon Alfa-n3
Dosage FormInjection
Route of AdministrationSUBCUTANEOUS
Marketing Start Date1989-10-10
Marketing CategoryBLA / BLA
Application NumberBLA103158
Labeler NameHemispherx Biopharma, Inc
Substance NameINTERFERON ALFA-N3
Active Ingredient Strength5000000 [arb'U]/mL
Pharm ClassesInterferon alpha [EPC],Interferon-alpha [Chemical/Ingredient]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 54746-001-01

0 mL in 1 VIAL, GLASS (54746-001-01)
Marketing Start Date1989-10-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 54746-001-01 [54746000101]

Alferon INJECTION
Marketing CategoryBLA
Application NumberBLA103158
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1989-10-10

Drug Details

Active Ingredients

IngredientStrength
INTERFERON ALFA-N35000000 [arb'U]/mL

OpenFDA Data

SPL SET ID:241ece31-e649-021a-e054-00144ff8d46c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 598014
  • 615136
  • Pharmacological Class

    • Interferon alpha [EPC]
    • Interferon-alpha [Chemical/Ingredient]

    Trademark Results [Alferon]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ALFERON
    ALFERON
    73608837 1427170 Live/Registered
    INTERFERON SCIENCES, INC.
    1986-07-10
    ALFERON
    ALFERON
    71456790 0400889 Dead/Cancelled
    DRIVER-HARRIS COMPANY
    1942-11-13

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