Package 68071-3884-2

Brand: latanoprost

Generic: latanoprost
NDC Package

Package Facts

Identity

Package NDC 68071-3884-2
Digits Only 6807138842
Product NDC 68071-3884
Description

1 BOTTLE in 1 CARTON (68071-3884-2) / 2.5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-08-13
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": "3c477d33-a8ca-d39f-e063-6294a90ac5f0", "openfda": {"nui": ["N0000175454", "M0017805"], "upc": ["0368071388428"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["3c47a089-2c72-f58c-e063-6294a90a4cce"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68071-3884-2)  / 2.5 mL in 1 BOTTLE", "package_ndc": "68071-3884-2", "marketing_start_date": "20250813"}], "brand_name": "Latanoprost", "product_id": "68071-3884_3c477d33-a8ca-d39f-e063-6294a90ac5f0", "dosage_form": "SOLUTION", "product_ndc": "68071-3884", "generic_name": "Latanoprost", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Latanoprost", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "ANDA091449", "marketing_category": "ANDA", "marketing_start_date": "20110107", "listing_expiration_date": "20261231"}