Package 30142-398-05

Brand: eye itch relief

Generic: ketotifen fumarate
NDC Package

Package Facts

Identity

Package NDC 30142-398-05
Digits Only 3014239805
Product NDC 30142-398
Description

1 BOTTLE in 1 CARTON (30142-398-05) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-06-01
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": "c9bce135-e1e4-4faa-b74c-22f69a060a3e", "openfda": {"upc": ["0041260103407"], "unii": ["HBD503WORO"], "rxcui": ["311237"], "spl_set_id": ["eb81286f-72b4-42b3-a596-439d0aeae93f"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-398-05)  / 5 mL in 1 BOTTLE", "package_ndc": "30142-398-05", "marketing_start_date": "20220601"}], "brand_name": "Eye Itch Relief", "product_id": "30142-398_c9bce135-e1e4-4faa-b74c-22f69a060a3e", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Inhibitor [EPC]"], "product_ndc": "30142-398", "generic_name": "ketotifen fumarate", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Eye Itch Relief", "active_ingredients": [{"name": "KETOTIFEN FUMARATE", "strength": ".25 mg/mL"}], "application_number": "NDA021996", "marketing_category": "NDA", "marketing_start_date": "20220601", "listing_expiration_date": "20261231"}