NDC 0008-1179

Torisel

Temsirolimus

Torisel is a Kit in the Human Prescription Drug category. It is labeled and distributed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The primary component is .

Product ID0008-1179_01c4c74e-da79-4a04-be8f-a8a123f7f670
NDC0008-1179
Product TypeHuman Prescription Drug
Proprietary NameTorisel
Generic NameTemsirolimus
Dosage FormKit
Marketing Start Date2007-07-01
Marketing CategoryNDA / NDA
Application NumberNDA022088
Labeler NameWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0008-1179-01

1 KIT in 1 CARTON (0008-1179-01) * 25 mL in 1 VIAL, SINGLE-USE (0008-1279-01) * 1.8 mL in 1 VIAL, SINGLE-USE (0008-1125-01)
Marketing Start Date2007-07-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0008-1179-01 [00008117901]

Torisel KIT
Marketing CategoryNDA
Application NumberNDA022088
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2007-07-01

Drug Details

OpenFDA Data

SPL SET ID:95b7dc92-2180-42f1-8699-3c28f609e674
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 722289
  • 725108
  • NDC Crossover Matching brand name "Torisel" or generic name "Temsirolimus"

    NDCBrand NameGeneric Name
    0008-1179Toriseltemsirolimus
    16729-223Temsirolimustemsirolimus
    65219-200TemsirolimusTemsirolimus

    Trademark Results [Torisel]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    TORISEL
    TORISEL
    78618928 3330991 Live/Registered
    WYETH LLC
    2005-04-28
    TORISEL
    TORISEL
    77227208 4074405 Live/Registered
    WYETH LLC
    2007-07-11

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