vyzulta

Generic: latanoprostene bunod

Labeler: bausch & lomb incorporated
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name vyzulta
Generic Name latanoprostene bunod
Labeler bausch & lomb incorporated
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

latanoprostene bunod .24 mg/mL

Manufacturer
Bausch & Lomb Incorporated

Identifiers & Regulatory

Product NDC 24208-504
Product ID 24208-504_12648511-1ae2-aaf8-e063-6394a90a2297
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA207795
Listing Expiration 2026-12-31
Marketing Start 2017-11-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208504
Hyphenated Format 24208-504

Supplemental Identifiers

RxCUI
1988394 1988399
UNII
I6393O0922

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name vyzulta (source: ndc)
Generic Name latanoprostene bunod (source: ndc)
Application Number NDA207795 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • .24 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (24208-504-01) / 2.5 mL in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (24208-504-02) / 2.5 mL in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (24208-504-05) / 5 mL in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (24208-504-06) / 5 mL in 1 BOTTLE
source: ndc

Packages (4)

24208-504-01 1 BOTTLE in 1 CARTON (24208-504-01) / 2.5 mL in 1 BOTTLE 24208-504-02 1 BOTTLE in 1 CARTON (24208-504-02) / 2.5 mL in 1 BOTTLE 24208-504-05 1 BOTTLE in 1 CARTON (24208-504-05) / 5 mL in 1 BOTTLE 24208-504-06 1 BOTTLE in 1 CARTON (24208-504-06) / 5 mL in 1 BOTTLE

Ingredients (1)

latanoprostene bunod (.24 mg/mL)

Linked Drug Pages (1)

Vyzulta ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "12648511-1ae2-aaf8-e063-6394a90a2297", "openfda": {"unii": ["I6393O0922"], "rxcui": ["1988394", "1988399"], "spl_set_id": ["60ce7900-a677-4fc2-88d0-1603baa9dbd4"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "1 BOTTLE in 1 CARTON (24208-504-01)  / 2.5 mL in 1 BOTTLE", "package_ndc": "24208-504-01", "marketing_start_date": "20180611"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (24208-504-02)  / 2.5 mL in 1 BOTTLE", "package_ndc": "24208-504-02", "marketing_start_date": "20180611"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (24208-504-05)  / 5 mL in 1 BOTTLE", "package_ndc": "24208-504-05", "marketing_start_date": "20171102"}, {"sample": true, "description": "1 BOTTLE in 1 CARTON (24208-504-06)  / 5 mL in 1 BOTTLE", "package_ndc": "24208-504-06", "marketing_start_date": "20171102"}], "brand_name": "Vyzulta", "product_id": "24208-504_12648511-1ae2-aaf8-e063-6394a90a2297", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "24208-504", "generic_name": "latanoprostene bunod", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vyzulta", "active_ingredients": [{"name": "LATANOPROSTENE BUNOD", "strength": ".24 mg/mL"}], "application_number": "NDA207795", "marketing_category": "NDA", "marketing_start_date": "20171102", "listing_expiration_date": "20261231"}