NDC 0004-0381

FUZEON

Enfuvirtide

FUZEON is a Kit in the Human Prescription Drug category. It is labeled and distributed by Genentech, Inc.. The primary component is .

Product ID0004-0381_0b811e50-d0e0-4679-8d14-d9c91e867334
NDC0004-0381
Product TypeHuman Prescription Drug
Proprietary NameFUZEON
Generic NameEnfuvirtide
Dosage FormKit
Marketing Start Date2012-04-10
Marketing CategoryNDA / NDA
Application NumberNDA021481
Labeler NameGenentech, Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0004-0381-40

1 KIT in 1 CARTON (0004-0381-40) * 1 mL in 1 VIAL, SINGLE-USE * 1 mL in 1 VIAL, SINGLE-DOSE
Marketing Start Date2012-04-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0004-0381-40 [00004038140]

FUZEON KIT
Marketing CategoryNDA
Application NumberNDA021481
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-04-10

Drug Details

OpenFDA Data

SPL SET ID:6935e846-d5a1-49e5-89a2-f8ebe4d5590d
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 404460
  • 401981

  • Trademark Results [FUZEON]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    FUZEON
    FUZEON
    76119460 2742964 Live/Registered
    Hoffmann-La Roche Inc.
    2000-08-30

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.