Package 72789-380-15

Brand: loratadine antihistamine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 72789-380-15
Digits Only 7278938015
Product NDC 72789-380
Description

15 TABLET in 1 BOTTLE, PLASTIC (72789-380-15)

Marketing

Marketing Status
Marketed Since 2024-02-07
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": "4bc0370f-21d9-1acb-e063-6394a90ad768", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["775885f9-0580-4eca-94d8-44fce1dcdccd"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (72789-380-15)", "package_ndc": "72789-380-15", "marketing_start_date": "20240207"}], "brand_name": "Loratadine antihistamine", "product_id": "72789-380_4bc0370f-21d9-1acb-e063-6394a90ad768", "dosage_form": "TABLET", "product_ndc": "72789-380", "generic_name": "Loratadine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20271231"}