Package 80425-0352-1

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 80425-0352-1
Digits Only 8042503521
Product NDC 80425-0352
Product ID 80425-0352_2a9c2eb6-a6de-f647-e063-6294a90a93fe
Description

30 TABLET in 1 BOTTLE (80425-0352-1)

Marketing

Marketing Status
Marketed Since 2023-07-31
Brand loratadine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Loratadine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a9c2eb6-a6de-f647-e063-6294a90a93fe", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["01cb43cf-57a9-f189-e063-6294a90afd88"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0352-1)", "package_ndc": "80425-0352-1", "marketing_start_date": "20230731"}], "brand_name": "Loratadine", "product_id": "80425-0352_2a9c2eb6-a6de-f647-e063-6294a90a93fe", "dosage_form": "TABLET", "product_ndc": "80425-0352", "generic_name": "loratadine", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA214684", "marketing_category": "ANDA", "marketing_start_date": "20230731", "listing_expiration_date": "20261231"}