Package 68016-088-10

Brand: loratadine odt

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 68016-088-10
Digits Only 6801608810
Product NDC 68016-088
Description

1 BLISTER PACK in 1 CARTON (68016-088-10) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-04-11
Brand loratadine odt
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38d1e80f-4bba-4acb-bc49-89bd3653c2cd", "openfda": {"upc": ["0358602744830"], "unii": ["7AJO3BO7QN"], "rxcui": ["311373"], "spl_set_id": ["7674009d-492d-4005-a652-f12b91428c0d"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68016-088-10)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "68016-088-10", "marketing_start_date": "20180411"}], "brand_name": "Loratadine ODT", "product_id": "68016-088_38d1e80f-4bba-4acb-bc49-89bd3653c2cd", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "68016-088", "generic_name": "Loratadine", "labeler_name": "Chain Drug Consortium, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine ODT", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA208477", "marketing_category": "ANDA", "marketing_start_date": "20180411", "listing_expiration_date": "20261231"}