latanoprost
Generic: latanoprost
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
latanoprost
Generic Name
latanoprost
Labeler
aurobindo pharma limited
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
latanoprost 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65862-872
Product ID
65862-872_cad9da15-f479-4b42-9d22-02c3f7dab1ba
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206519
Listing Expiration
2026-12-31
Marketing Start
2019-09-03
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65862872
Hyphenated Format
65862-872
Supplemental Identifiers
RxCUI
UPC
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
ANDA206519 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 1 BOTTLE in 1 CARTON (65862-872-25) / 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": "cad9da15-f479-4b42-9d22-02c3f7dab1ba", "openfda": {"nui": ["N0000175454", "M0017805"], "upc": ["0365862872258"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["19cdfef0-b770-4758-8f59-1769e4b6119c"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (65862-872-25) / 2.5 mL in 1 BOTTLE", "package_ndc": "65862-872-25", "marketing_start_date": "20190903"}], "brand_name": "Latanoprost", "product_id": "65862-872_cad9da15-f479-4b42-9d22-02c3f7dab1ba", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "65862-872", "generic_name": "Latanoprost", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Latanoprost", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "ANDA206519", "marketing_category": "ANDA", "marketing_start_date": "20190903", "listing_expiration_date": "20261231"}