Package 68016-053-30

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 68016-053-30
Digits Only 6801605330
Product NDC 68016-053
Description

1 BLISTER PACK in 1 CARTON (68016-053-30) / 30 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-04-01
Brand loratadine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a409885-2a3e-34d8-e063-6394a90aa4d9", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["665078"], "spl_set_id": ["dc22862e-fe91-4900-8c2b-1ca45aeedbf0"], "manufacturer_name": ["Premier Value"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68016-053-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "68016-053-10", "marketing_start_date": "20180401"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68016-053-30)  / 30 TABLET in 1 BLISTER PACK", "package_ndc": "68016-053-30", "marketing_start_date": "20180401"}], "brand_name": "Loratadine", "product_id": "68016-053_2a409885-2a3e-34d8-e063-6394a90aa4d9", "dosage_form": "TABLET", "product_ndc": "68016-053", "generic_name": "Loratadine", "labeler_name": "Premier Value", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/1"}], "application_number": "ANDA210088", "marketing_category": "ANDA", "marketing_start_date": "20180401", "listing_expiration_date": "20261231"}