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 ID: 0008-1179_01c4c74e-da79-4a04-be8f-a8a123f7f670
• NDC: 0008-1179
• Product Type: Human Prescription Drug
• Proprietary Name: Torisel
• Generic Name: Temsirolimus
• Dosage Form: Kit
• Marketing Start Date: 2007-07-01
• Marketing Category: NDA / NDA
• Application Number: NDA022088
• Labeler Name: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

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 Date: 2007-07-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0008-1179-01 [00008117901]

Torisel KIT

• Marketing Category: NDA
• Application Number: NDA022088
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2007-07-01

Drug Details

OpenFDA Data

• SPL SET ID: 95b7dc92-2180-42f1-8699-3c28f609e674
• Manufacturer:
  • Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 722289
  • 725108

NDC Crossover Matching brand name "Torisel" or generic name "Temsirolimus"

NDC	Brand Name	Generic Name
0008-1179	Torisel	temsirolimus
16729-223	Temsirolimus	temsirolimus
65219-200	Temsirolimus	Temsirolimus