latanoprost
Generic: latanoprost
Labeler: mylan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
latanoprost
Generic Name
latanoprost
Labeler
mylan pharmaceuticals inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
latanoprost 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
59762-0333
Product ID
59762-0333_a25c5b35-f731-4e01-bd83-d455d9e12779
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020597
Listing Expiration
2026-12-31
Marketing Start
2010-11-15
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
597620333
Hyphenated Format
59762-0333
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
NDA020597 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (59762-0333-2) / 2.5 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "a25c5b35-f731-4e01-bd83-d455d9e12779", "openfda": {"nui": ["N0000175454", "M0017805"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["463ecfde-5acb-4983-969d-0c0021bfbf48"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (59762-0333-2) / 2.5 mL in 1 BOTTLE, DROPPER", "package_ndc": "59762-0333-2", "marketing_start_date": "20101115"}], "brand_name": "Latanoprost", "product_id": "59762-0333_a25c5b35-f731-4e01-bd83-d455d9e12779", "dosage_form": "SOLUTION", "product_ndc": "59762-0333", "generic_name": "Latanoprost", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Latanoprost", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "NDA020597", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20101115", "listing_expiration_date": "20261231"}