Package 45802-650-65

Brand: loratadine antihistamine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 45802-650-65
Digits Only 4580265065
Product NDC 45802-650
Description

1 BOTTLE in 1 CARTON (45802-650-65) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2008-10-15
Brand loratadine antihistamine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "497be46d-b620-41ae-bac0-95ef0bd94fe4", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["c72d8a30-520e-4d25-8f02-0c891e070a1a"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (45802-650-65)  / 30 TABLET in 1 BOTTLE", "package_ndc": "45802-650-65", "marketing_start_date": "20081015"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (45802-650-75)  / 90 TABLET in 1 BOTTLE", "package_ndc": "45802-650-75", "marketing_end_date": "20261231", "marketing_start_date": "20230915"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (45802-650-78)  / 100 TABLET in 1 BOTTLE", "package_ndc": "45802-650-78", "marketing_start_date": "20091007"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (45802-650-87)  / 300 TABLET in 1 BOTTLE", "package_ndc": "45802-650-87", "marketing_start_date": "20081028"}], "brand_name": "Loratadine antihistamine", "product_id": "45802-650_497be46d-b620-41ae-bac0-95ef0bd94fe4", "dosage_form": "TABLET", "product_ndc": "45802-650", "generic_name": "Loratadine", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "brand_name_suffix": "antihistamine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076301", "marketing_category": "ANDA", "marketing_start_date": "20081015", "listing_expiration_date": "20261231"}