latanoprost
Generic: latanoprost
Labeler: bausch & lomb incorporatedDrug Facts
Product Profile
Brand Name
latanoprost
Generic Name
latanoprost
Labeler
bausch & lomb incorporated
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
latanoprost 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24208-463
Product ID
24208-463_41d52f40-88d7-8f69-e063-6394a90ab025
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201006
Listing Expiration
2026-12-31
Marketing Start
2011-03-22
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24208463
Hyphenated Format
24208-463
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
latanoprost (source: ndc)
Generic Name
latanoprost (source: ndc)
Application Number
ANDA201006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 1 BOTTLE in 1 CARTON (24208-463-25) / 2.5 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "41d52f40-88d7-8f69-e063-6394a90ab025", "openfda": {"nui": ["N0000175454", "M0017805"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["68aaacbe-98c5-450b-9bf4-4809d7ad2ca0"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (24208-463-25) / 2.5 mL in 1 BOTTLE", "package_ndc": "24208-463-25", "marketing_start_date": "20110322"}], "brand_name": "Latanoprost", "product_id": "24208-463_41d52f40-88d7-8f69-e063-6394a90ab025", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "24208-463", "generic_name": "latanoprost", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Latanoprost", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "ANDA201006", "marketing_category": "ANDA", "marketing_start_date": "20110322", "listing_expiration_date": "20261231"}