NDC 50242-080

LUCENTIS

Ranibizumab

LUCENTIS is a Intravitreal Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Genentech, Inc.. The primary component is Ranibizumab.

Product ID50242-080_115f8246-b87c-49aa-b411-e67afecdced9
NDC50242-080
Product TypeHuman Prescription Drug
Proprietary NameLUCENTIS
Generic NameRanibizumab
Dosage FormInjection, Solution
Route of AdministrationINTRAVITREAL
Marketing Start Date2006-06-30
Marketing CategoryBLA / BLA
Application NumberBLA125156
Labeler NameGenentech, Inc.
Substance NameRANIBIZUMAB
Active Ingredient Strength10 mg/mL
Pharm ClassesVascular Endothelial Growth Factor Inhibitors [MoA],Vascular Endothelial Growth Factor Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 50242-080-01

1 VIAL, SINGLE-USE in 1 CARTON (50242-080-01) > .05 mL in 1 VIAL, SINGLE-USE
Marketing Start Date2006-06-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50242-080-03 [50242008003]

LUCENTIS INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA125156
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-10-13

NDC 50242-080-86 [50242008086]

LUCENTIS INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA125156
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2009-09-04
Marketing End Date2018-04-30

NDC 50242-080-01 [50242008001]

LUCENTIS INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA125156
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-06-30

NDC 50242-080-02 [50242008002]

LUCENTIS INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA125156
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-11-28

NDC 50242-080-88 [50242008088]

LUCENTIS INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA125156
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-10-13

Drug Details

Active Ingredients

IngredientStrength
RANIBIZUMAB10 mg/mL

OpenFDA Data

SPL SET ID:de4e66cc-ca05-4dc9-8262-e00e9b41c36d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1306074
  • 1864423
  • 1306076
  • 2045502
  • 2045501
  • 1864425
  • 643193
  • 644301
  • Pharmacological Class

    • Vascular Endothelial Growth Factor Inhibitors [MoA]
    • Vascular Endothelial Growth Factor Inhibitor [EPC]

    NDC Crossover Matching brand name "LUCENTIS" or generic name "Ranibizumab"

    NDCBrand NameGeneric Name
    50242-080LUCENTISRANIBIZUMAB
    50242-082LUCENTISRANIBIZUMAB
    64406-019Byoovizranibizumab
    50242-078SusvimoRanibizumab

    Trademark Results [LUCENTIS]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    LUCENTIS
    LUCENTIS
    98765698 not registered Live/Pending
    Jun Luo
    2024-09-23
    LUCENTIS
    LUCENTIS
    78238446 3169327 Live/Registered
    GENENTECH, INC.
    2003-04-16

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