Torisel
- Product NDC
- 0008-1179
- 11-digit product format
- 000081179
- Labeler code
- 0008
- Product ID
- 0008-1179_8731b3b1-29d9-46b1-a443-822d8057f773
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- temsirolimus
- Dosage form
- KIT
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Application
- NDA022088
- Marketing category
- NDA
- Marketing start
- 2007-07-01
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Torisel
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 722289, 725108 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0008-1179-01 | Torisel | 1 in 1 CARTON | KIT | 1 | | 39 |
| 0008-1279-01 | Torisel | 25 mL in 1 VIAL, SINGLE-USE | INJECTION, SOLUTION, CONCENTRATE | 25 mL | 25 mg in 1mL | 39 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0008-1179 | TORISEL (TEMSIROLIMUS) KIT [WYETH PHARMACEUTICALS LLC, A SUBSIDIARY OF PFIZER INC.] | 38 | Current NDC, Legacy NDC, 2 package rows | 20250323_95b7dc92-2180-42f1-8699-3c28f609e674.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0008-1179-01 | 00008117901 | 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) | 1 kit | 2007-07-01 | 0000-00-00 | No | No | Current |
| 0008-1279-01 | 00008127901 | 25 mL in 1 VIAL, SINGLE-USE | 25 ml | | | | | Historical |