visudyne

Generic: verteporfin for injection

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

Drug Facts

Product Profile

Brand Name visudyne
Generic Name verteporfin for injection
Labeler bausch & lomb incorporated
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

verteporfin 15 mg/1

Manufacturer
Bausch & Lomb Incorporated

Identifiers & Regulatory

Product NDC 24208-560
Product ID 24208-560_f48ec619-2eda-4360-9c67-bb79bdd00353
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021119
Listing Expiration 2026-12-31
Marketing Start 2000-04-12

Pharmacologic Class

Established (EPC)
photoenhancer [epc]
Mechanism of Action
photoabsorption [moa]
Physiologic Effect
photosensitizing activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208560
Hyphenated Format 24208-560

Supplemental Identifiers

RxCUI
313595 351914
UNII
0X9PA28K43
NUI
N0000010217 N0000175540 N0000009801

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 visudyne (source: ndc)
Generic Name verteporfin for injection (source: ndc)
Application Number NDA021119 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (24208-560-15)
source: ndc

Packages (1)

Ingredients (1)

verteporfin (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f48ec619-2eda-4360-9c67-bb79bdd00353", "openfda": {"nui": ["N0000010217", "N0000175540", "N0000009801"], "unii": ["0X9PA28K43"], "rxcui": ["313595", "351914"], "spl_set_id": ["2f0a34ce-3c57-4ac8-b28e-512be807272f"], "pharm_class_pe": ["Photosensitizing Activity [PE]"], "pharm_class_epc": ["Photoenhancer [EPC]"], "pharm_class_moa": ["Photoabsorption [MoA]"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (24208-560-15)", "package_ndc": "24208-560-15", "marketing_start_date": "20230227"}], "brand_name": "Visudyne", "product_id": "24208-560_f48ec619-2eda-4360-9c67-bb79bdd00353", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Photoabsorption [MoA]", "Photoenhancer [EPC]", "Photosensitizing Activity [PE]"], "product_ndc": "24208-560", "generic_name": "verteporfin for injection", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Visudyne", "active_ingredients": [{"name": "VERTEPORFIN", "strength": "15 mg/1"}], "application_number": "NDA021119", "marketing_category": "NDA", "marketing_start_date": "20000412", "listing_expiration_date": "20261231"}