TECENTRIQ
- Product NDC
- 50242-917
- 11-digit product format
- 502420917
- Labeler code
- 50242
- Product ID
- 50242-917_4b922b35-c401-4189-a8b2-9f9a820878db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atezolizumab
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Genentech, Inc.
- Application
- BLA761034
- Marketing category
- BLA
- Marketing start
- 2016-05-18
- Substance
- ATEZOLIZUMAB
- Active strength
- 1200 mg/20mL
- Pharmacologic classes
- Antibodies [CS], Antibodies, Monoclonal [CS], Antibodies, Monoclonal, Humanized [CS], Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TECENTRIQ
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ATEZOLIZUMAB | 1200 mg/20mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 52CMI0WC3Y |
| Rxcui | 1792780, 1792785, 2119695, 2119696 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50242-917-01 | TECENTRIQ | 20 mL in 1 VIAL, SINGLE-USE | INJECTION, SOLUTION | 20 | | 45 |
| 50242-917-01 | TECENTRIQ | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 45 |
| 50242-917-86 | TECENTRIQ | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 45 |
| 50242-917-86 | TECENTRIQ | 20 mL in 1 VIAL, SINGLE-USE | INJECTION, SOLUTION | 20 | | 45 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50242-917 | TECENTRIQ (ATEZOLIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 37 | Current NDC, Legacy NDC, 4 package rows | 20241122_6fa682c9-a312-4932-9831-f286908660ee.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50242-917-01 | 50242091701 | 1 VIAL, SINGLE-USE in 1 CARTON (50242-917-01) / 20 mL in 1 VIAL, SINGLE-USE | 2016-05-18 | 0000-00-00 | No | No | Current |
| 50242-917-86 | 50242091786 | 1 VIAL, SINGLE-USE in 1 CARTON (50242-917-86) / 20 mL in 1 VIAL, SINGLE-USE | 2016-08-11 | 0000-00-00 | Yes | No | Current |