Package 42571-499-06

Brand: latanoprost

Generic: latanoprost
NDC Package

Package Facts

Identity

Package NDC 42571-499-06
Digits Only 4257149906
Product NDC 42571-499
Description

1 BOTTLE in 1 CARTON (42571-499-06) / 2.5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2026-01-22
Brand latanoprost
Generic latanoprost
Sample Package No

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"}