LUCENTIS
- Product NDC
- 50242-080
- 11-digit product format
- 502420080
- Labeler code
- 50242
- Product ID
- 50242-080_71a6df7b-906b-4de9-ad4f-200285958cdc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RANIBIZUMAB
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVITREAL
- Labeler
- Genentech, Inc.
- Application
- BLA125156
- Marketing category
- BLA
- Marketing start
- 2006-06-30
- Substance
- RANIBIZUMAB
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Vascular Endothelial Growth Factor Inhibitor [EPC], Vascular Endothelial Growth Factor Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LUCENTIS
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| RANIBIZUMAB | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZL1R02VT79 |
| Rxcui | 1864423, 1864425, 2045501, 2045502 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50242-080-03 | LUCENTIS | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 27 |
| 50242-080-03 | LUCENTIS | 0.05 mL in 1 SYRINGE, GLASS | INJECTION, SOLUTION | 0.05 | | 27 |
| 50242-080-88 | LUCENTIS | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 27 |
| 50242-080-88 | LUCENTIS | 0.05 mL in 1 SYRINGE, GLASS | INJECTION, SOLUTION | 0.05 | | 27 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| RANIBIZUMAB | ACTIVE INGREDIENT | ZL1R02VT79 | LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 9 | |
| RANIBIZUMAB | ACTIVE MOIETY | ZL1R02VT79 | LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 9 | |
| HISTIDINE | INACTIVE INGREDIENT | 4QD397987E | LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 9 | |
| HISTIDINE MONOHYDROCHLORIDE | INACTIVE INGREDIENT | 1D5Q932XM6 | LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 9 | |
| POLYSORBATE 20 | INACTIVE INGREDIENT | 7T1F30V5YH | LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 9 | |
| TREHALOSE DIHYDRATE | INACTIVE INGREDIENT | 7YIN7J07X4 | LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 9 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 9 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50242-080 | LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.] | 25 | Current NDC, Legacy NDC, 4 package rows | 20241123_de4e66cc-ca05-4dc9-8262-e00e9b41c36d.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 |
|---|
| 50242-080-01 | 50242008001 | 1 VIAL, SINGLE-USE in 1 CARTON (50242-080-01) > .05 mL in 1 VIAL, SINGLE-USE | 2006-06-30 | 0000-00-00 | No | No | Current |
| 50242-080-02 | 50242008002 | 1 VIAL, SINGLE-USE in 1 CARTON (50242-080-02) > .05 mL in 1 VIAL, SINGLE-USE | 2016-11-28 | 0000-00-00 | No | No | Current |
| 50242-080-03 | 50242008003 | 1 SYRINGE, GLASS in 1 CARTON (50242-080-03) / .05 mL in 1 SYRINGE, GLASS | 2016-10-13 | 0000-00-00 | No | No | Current |
| 50242-080-88 | 50242008088 | 1 SYRINGE, GLASS in 1 CARTON (50242-080-88) / .05 mL in 1 SYRINGE, GLASS | 2016-10-13 | 0000-00-00 | Yes | No | Current |