Package 70000-0124-1

Brand: eye itch relief

Generic: ketotifen fumarate
NDC Package

Package Facts

Identity

Package NDC 70000-0124-1
Digits Only 7000001241
Product NDC 70000-0124
Description

1 BOTTLE, DROPPER in 1 CARTON (70000-0124-1) / 5 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Discontinued 2028-03-31
Brand eye itch relief
Generic ketotifen fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "0c2e7ac9-3977-48ba-995c-004dba0d0ad5", "openfda": {"upc": ["0096295128901"], "unii": ["HBD503WORO"], "rxcui": ["311237"], "spl_set_id": ["add414c5-b6c5-4bb5-8d8a-ddc507a27131"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC. DBA LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (70000-0124-1)  / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "70000-0124-1", "marketing_end_date": "20280331", "marketing_start_date": "20170118"}], "brand_name": "Eye Itch Relief", "product_id": "70000-0124_0c2e7ac9-3977-48ba-995c-004dba0d0ad5", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Inhibitor [EPC]"], "product_ndc": "70000-0124", "generic_name": "Ketotifen Fumarate", "labeler_name": "CARDINAL HEALTH 110, LLC. DBA LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Eye Itch Relief", "active_ingredients": [{"name": "KETOTIFEN FUMARATE", "strength": ".35 mg/mL"}], "application_number": "ANDA077958", "marketing_category": "ANDA", "marketing_end_date": "20280331", "marketing_start_date": "20170118"}