torisel
Generic: temsirolimus
Labeler: wyeth pharmaceuticals llc, a subsidiary of pfizer inc.Drug Facts
Product Profile
Brand Name
torisel
Generic Name
temsirolimus
Labeler
wyeth pharmaceuticals llc, a subsidiary of pfizer inc.
Dosage Form
KIT
Manufacturer
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
Packaging Origin
Original Packager
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
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)
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"}