latanoprost
Generic: latanoprost
Labeler: micro labs limitedDrug Facts
Product Profile
Brand Name
latanoprost
Generic Name
latanoprost
Labeler
micro labs limited
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
latanoprost 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
42571-499
Product ID
42571-499_48f3aae3-9e51-3c90-e063-6294a90a3a8b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA219306
Listing Expiration
2027-12-31
Marketing Start
2026-01-22
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42571499
Hyphenated Format
42571-499
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
ANDA219306 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 1 BOTTLE in 1 CARTON (42571-499-06) / 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": "48f3aae3-9e51-3c90-e063-6294a90a3a8b", "openfda": {"nui": ["N0000175454", "M0017805"], "upc": ["0342571499068"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["298fc762-f4d4-47cb-a7a2-b5dc7f965c7f"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (42571-499-06) / 2.5 mL in 1 BOTTLE", "package_ndc": "42571-499-06", "marketing_start_date": "20260122"}], "brand_name": "Latanoprost", "product_id": "42571-499_48f3aae3-9e51-3c90-e063-6294a90a3a8b", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "42571-499", "generic_name": "Latanoprost", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Latanoprost", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "ANDA219306", "marketing_category": "ANDA", "marketing_start_date": "20260122", "listing_expiration_date": "20271231"}