Package 65785-125-01

Brand: uline eyewash

Generic: eyewash
NDC Package

Package Facts

Identity

Package NDC 65785-125-01
Digits Only 6578512501
Product NDC 65785-125
Description

473 mL in 1 BOTTLE, UNIT-DOSE (65785-125-01)

Marketing

Marketing Status
Marketed Since 2024-04-01
Brand uline eyewash
Generic eyewash
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "445cc5b0-291c-a344-e063-6394a90a0298", "openfda": {"unii": ["059QF0KO0R"], "rxcui": ["1151101"], "spl_set_id": ["2d7f22d2-320b-6af1-e063-6294a90addc6"], "manufacturer_name": ["Niagara Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, UNIT-DOSE (65785-125-01)", "package_ndc": "65785-125-01", "marketing_start_date": "20240401"}, {"sample": false, "description": "946 mL in 1 BOTTLE, UNIT-DOSE (65785-125-02)", "package_ndc": "65785-125-02", "marketing_start_date": "20240401"}], "brand_name": "ULINE Eyewash", "product_id": "65785-125_445cc5b0-291c-a344-e063-6394a90a0298", "dosage_form": "SOLUTION", "product_ndc": "65785-125", "generic_name": "Eyewash", "labeler_name": "Niagara Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ULINE Eyewash", "active_ingredients": [{"name": "WATER", "strength": "465 mL/473mL"}], "application_number": "NDA022305", "marketing_category": "NDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}