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 UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
ZL1R02VT79	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1864423	Internal RxNorm lookup
1864425	Internal RxNorm lookup
2045501	Internal RxNorm lookup
2045502	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
de4e66cc-ca05-4dc9-8262-e00e9b41c36d	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
02a7bcab-2730-41aa-8529-7c6226e65bab	Product name	1	20220516
d6b571bf-7bed-4e31-93c1-5553936e1c45	Product name	1	20220315
da4394b8-eff9-4932-92e2-14d8feb38640	Product name	1	20161208
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50242-080-01	ML - Milliliter	50242-080	3edf6fbd-66cc-4748-a47e-df21c2a9c2ec	1	2012-07-24
50242-080-02	ML - Milliliter	50242-080	60f30cd6-cf55-44c7-bee7-66fca365fffc	1	2017-05-03
50242-080-03	ML - Milliliter	50242-080	2c65242a-61ea-46d4-9f68-902cad8f19b7	1	2017-03-06
50242-080-86	ML - Milliliter	50242-080	20a2e0d8-db2d-42e0-9084-f754df3e6982	1	2019-02-13
50242-080-88	ML - Milliliter	50242-080	7d32858a-96d4-42f1-b0be-a05fd851506c	1	2019-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
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

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
LUCENTIS	RANIBIZUMAB	Genentech, Inc.	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	2025-11-21	Warnings, Adverse reactions	Exact identifier application number: BLA125156 ndc (product): 50242-080

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLA	Proprietary name	Proper name	License type	Status	Latest source
125156	Lucentis	ranibizumab	351(a)	Disc*	2026-07-01

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
ZL1R02VT79	RANIBIZUMAB	347396-82-1	RANIBIZUMAB

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2045502	Lucentis 0.3 MG in 0.05 ML Prefilled Syringe	PSN	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
1864425	Lucentis 0.5 MG in 0.05 ML Prefilled Syringe	PSN	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
2045501	ranibizumab 0.3 MG in 0.05 ML Prefilled Syringe	PSN	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
1864423	ranibizumab 0.5 MG in 0.05 ML Prefilled Syringe	PSN	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
1864425	0.05 ML ranibizumab 10 MG/ML Prefilled Syringe [Lucentis]	SBD	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
2045502	0.05 ML ranibizumab 6 MG/ML Prefilled Syringe [Lucentis]	SBD	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
1864423	0.05 ML ranibizumab 10 MG/ML Prefilled Syringe	SCD	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
2045501	0.05 ML ranibizumab 6 MG/ML Prefilled Syringe	SCD	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
1864425	0.05 ML Lucentis 10 MG/ML Prefilled Syringe	SY	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
2045502	0.05 ML Lucentis 6 MG/ML Prefilled Syringe	SY	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
2045502	Lucentis 0.3 MG per 0.05 ML Prefilled Syringe	SY	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
1864425	Lucentis 0.5 MG per 0.05 ML Prefilled Syringe	SY	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
2045501	ranibizumab 0.3 MG per 0.05 ML Prefilled Syringe	SY	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27
1864423	ranibizumab 0.5 MG per 0.05 ML Prefilled Syringe	SY	de4e66cc-ca05-4dc9-8262-e00e9b41c36d	27

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
LUCENTIS	Genentech, Inc. \| Roche Singapore Technical Operations Pte. Ltd.	2025-11-21	HUMAN PRESCRIPTION DRUG LABEL	27