Package 11822-5533-1

Brand: eye itch releif

Generic: ketotifen fumarate
NDC Package

Package Facts

Identity

Package NDC 11822-5533-1
Digits Only 1182255331
Product NDC 11822-5533
Description

1 BOTTLE, DROPPER in 1 CARTON (11822-5533-1) / 10 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 2022-04-01
Brand eye itch releif
Generic ketotifen fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "1ddd5a87-3863-532b-e063-6394a90ab8bf", "openfda": {"unii": ["HBD503WORO"], "rxcui": ["311237"], "spl_set_id": ["6a7be1e9-27ff-44d8-85ed-fc1b0017180e"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (11822-5533-1)  / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "11822-5533-1", "marketing_start_date": "20220401"}], "brand_name": "Eye Itch Releif", "product_id": "11822-5533_1ddd5a87-3863-532b-e063-6394a90ab8bf", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Inhibitor [EPC]"], "product_ndc": "11822-5533", "generic_name": "Ketotifen Fumarate", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Eye Itch Releif", "active_ingredients": [{"name": "KETOTIFEN FUMARATE", "strength": ".25 mg/mL"}], "application_number": "NDA021996", "marketing_category": "NDA", "marketing_start_date": "20220401", "listing_expiration_date": "20261231"}