Package 68210-4110-1

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 68210-4110-1
Digits Only 6821041101
Product NDC 68210-4110
Product ID 68210-4110_292df514-5dba-2a76-e063-6394a90acee6
Description

365 TABLET in 1 BOTTLE (68210-4110-1)

Marketing

Marketing Status
Marketed Since 2020-09-11
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": "292df514-5dba-2a76-e063-6394a90acee6", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["af0cdab2-27a4-5f30-e053-2a95a90a5e71"], "manufacturer_name": ["Spirit Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "365 TABLET in 1 BOTTLE (68210-4110-1)", "package_ndc": "68210-4110-1", "marketing_start_date": "20200911"}], "brand_name": "Loratadine", "product_id": "68210-4110_292df514-5dba-2a76-e063-6394a90acee6", "dosage_form": "TABLET", "product_ndc": "68210-4110", "generic_name": "Loratadine", "labeler_name": "Spirit Pharmaceuticals 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": "20200911", "listing_expiration_date": "20261231"}