Package 58151-419-35

Brand: xalatan

Generic: latanoprost
NDC Package

Package Facts

Identity

Package NDC 58151-419-35
Digits Only 5815141935
Product NDC 58151-419
Description

1 BOTTLE, DROPPER in 1 CARTON (58151-419-35) / 2.5 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 2024-10-22
Brand xalatan
Generic latanoprost
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "45489b8b-2aab-4336-8552-1524493289f9", "openfda": {"nui": ["N0000175454", "M0017805"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072", "542527"], "spl_set_id": ["a98595b3-9f47-48e0-b18d-550a2095f264"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (58151-419-35)  / 2.5 mL in 1 BOTTLE, DROPPER", "package_ndc": "58151-419-35", "marketing_start_date": "20241022"}], "brand_name": "XALATAN", "product_id": "58151-419_45489b8b-2aab-4336-8552-1524493289f9", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "58151-419", "generic_name": "Latanoprost", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "XALATAN", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "NDA020597", "marketing_category": "NDA", "marketing_start_date": "20241022", "listing_expiration_date": "20261231"}