Package 80513-711-01

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 80513-711-01
Digits Only 8051371101
Product NDC 80513-711
Product ID 80513-711_2efad4c4-593e-fa4d-e063-6294a90a0ebc
Description

100 TABLET in 1 BOTTLE (80513-711-01)

Marketing

Marketing Status
Marketed Since 2024-01-01
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": "2efad4c4-593e-fa4d-e063-6294a90a0ebc", "openfda": {"upc": ["0380513001184"], "unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["e96b4671-82dc-4cc6-a8bf-ef6f1efd8a7d"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (80513-711-01)", "package_ndc": "80513-711-01", "marketing_start_date": "20240101"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (80513-711-03)", "package_ndc": "80513-711-03", "marketing_start_date": "20240807"}], "brand_name": "Loratadine", "product_id": "80513-711_2efad4c4-593e-fa4d-e063-6294a90a0ebc", "dosage_form": "TABLET", "product_ndc": "80513-711", "generic_name": "Loratadine", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA210722", "marketing_category": "ANDA", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}