Package 70000-0053-1

Brand: eye allergy itch relief

Generic: olopatadine hydrochloride ophthalmic
NDC Package

Package Facts

Identity

Package NDC 70000-0053-1
Digits Only 7000000531
Product NDC 70000-0053
Description

1 BOTTLE, PLASTIC in 1 CARTON (70000-0053-1) / 2.5 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2021-01-15
Brand eye allergy itch relief
Generic olopatadine hydrochloride ophthalmic
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "a751380b-de68-03ed-5b9c-15596d15d3bd", "openfda": {"unii": ["2XG66W44KF"], "rxcui": ["1111343"], "spl_set_id": ["135bb2de-b2c0-6f0c-6204-3acbb48dcfbd"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC. DBA LEADER"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (70000-0053-1)  / 2.5 mL in 1 BOTTLE, PLASTIC", "package_ndc": "70000-0053-1", "marketing_start_date": "20210115"}], "brand_name": "Eye Allergy Itch Relief", "product_id": "70000-0053_a751380b-de68-03ed-5b9c-15596d15d3bd", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Histamine Release [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Histamine-1 Receptor Inhibitor [EPC]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "70000-0053", "generic_name": "Olopatadine Hydrochloride Ophthalmic", "labeler_name": "CARDINAL HEALTH 110, LLC. DBA LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Eye Allergy Itch Relief", "active_ingredients": [{"name": "OLOPATADINE HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA209752", "marketing_category": "ANDA", "marketing_start_date": "20210115", "listing_expiration_date": "20261231"}