LUCENTIS

Product NDC: 50242-082
11-digit product format: 502420082
Labeler code: 50242
Product ID: 50242-082_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: 2012-08-10
Substance: RANIBIZUMAB
Active strength: 6 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

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated 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): 50242-082

Additional Listing Data#

Finished product: Yes
Brand name base: LUCENTIS
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
RANIBIZUMAB	6 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
50242-082-03	LUCENTIS	0.05 mL in 1 SYRINGE, GLASS	INJECTION, SOLUTION	0.05	27
50242-082-03	LUCENTIS	1 in 1 CARTON	INJECTION, SOLUTION	1	27
50242-082-88	LUCENTIS	0.05 mL in 1 SYRINGE, GLASS	INJECTION, SOLUTION	0.05	27
50242-082-88	LUCENTIS	1 in 1 CARTON	INJECTION, SOLUTION	1	27

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50242-082-01	ML - Milliliter	50242-082	f448fdd1-c5af-4c96-9088-93f32b13052b	1	2013-02-13
50242-082-02	ML - Milliliter	50242-082	23379737-fca7-44cd-8198-3f3843cf6f0e	1	2017-05-03
50242-082-03	ML - Milliliter	50242-082	15146b97-2b0f-4922-8210-10ab45f7c968	1	2018-04-19
50242-082-87	ML - Milliliter	50242-082	83964095-5900-4e27-92bf-0e10801af5a9	1	2019-02-13
50242-082-88	ML - Milliliter	50242-082	4defc096-46eb-42ea-9067-2a2d90fce382	1	2019-05-02

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
50242-082	LUCENTIS (RANIBIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.]	25	Current NDC, Legacy NDC, 4 package rows	20241123_de4e66cc-ca05-4dc9-8262-e00e9b41c36d.zip

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*	2026-06-01

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
50242-082-01	50242008201	1 VIAL, SINGLE-USE in 1 CARTON (50242-082-01) > .05 mL in 1 VIAL, SINGLE-USE	2012-08-10	0000-00-00	No	No	Current
50242-082-02	50242008202	1 VIAL, SINGLE-USE in 1 CARTON (50242-082-02) > .05 mL in 1 VIAL, SINGLE-USE	2016-11-28	0000-00-00	No	No	Current
50242-082-03	50242008203	1 SYRINGE, GLASS in 1 CARTON (50242-082-03) / .05 mL in 1 SYRINGE, GLASS	2018-03-20	0000-00-00	No	No	Current
50242-082-87	50242008287	1 VIAL, SINGLE-USE in 1 CARTON (50242-082-87) > .05 mL in 1 VIAL, SINGLE-USE	2017-02-28	0000-00-00	Yes	No	Current
50242-082-88	50242008288	1 SYRINGE, GLASS in 1 CARTON (50242-082-88) / .05 mL in 1 SYRINGE, GLASS	2018-03-20	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