torisel

Generic: temsirolimus

Labeler: wyeth pharmaceuticals llc, a subsidiary of pfizer inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name torisel
Generic Name temsirolimus
Labeler wyeth pharmaceuticals llc, a subsidiary of pfizer inc.
Dosage Form KIT
Manufacturer
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

Identifiers & Regulatory

Product NDC 0008-1179
Product ID 0008-1179_8731b3b1-29d9-46b1-a443-822d8057f773
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022088
Listing Expiration 2026-12-31
Marketing Start 2007-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00081179
Hyphenated Format 0008-1179

Supplemental Identifiers

RxCUI
722289 725108

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name torisel (source: ndc)
Generic Name temsirolimus (source: ndc)
Application Number NDA022088 (source: ndc)

Resolved Composition

Strengths
  • 25 mg/ml
  • 0.2 ml
  • 1.8 ml
source: label
Packaging
  • 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)
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "8731b3b1-29d9-46b1-a443-822d8057f773", "openfda": {"rxcui": ["722289", "725108"], "spl_set_id": ["95b7dc92-2180-42f1-8699-3c28f609e674"], "manufacturer_name": ["Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "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)", "package_ndc": "0008-1179-01", "marketing_start_date": "20070701"}], "brand_name": "Torisel", "product_id": "0008-1179_8731b3b1-29d9-46b1-a443-822d8057f773", "dosage_form": "KIT", "product_ndc": "0008-1179", "generic_name": "temsirolimus", "labeler_name": "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Torisel", "application_number": "NDA022088", "marketing_category": "NDA", "marketing_start_date": "20070701", "listing_expiration_date": "20261231"}