Package 58602-830-83

Brand: loratadine odt

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 58602-830-83
Digits Only 5860283083
Product NDC 58602-830
Product ID 58602-830_5c099ee7-0679-45af-ac3d-d8e77d12e809
Description

1 BLISTER PACK in 1 CARTON (58602-830-83) / 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)

Loratadine ODT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5c099ee7-0679-45af-ac3d-d8e77d12e809", "openfda": {"upc": ["0358602830830"], "unii": ["7AJO3BO7QN"], "rxcui": ["311373"], "spl_set_id": ["1ba8e521-0b0f-419c-b7c3-fa9586f83f36"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (58602-830-83)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "58602-830-83", "marketing_start_date": "20180411"}], "brand_name": "Loratadine ODT", "product_id": "58602-830_5c099ee7-0679-45af-ac3d-d8e77d12e809", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "58602-830", "generic_name": "Loratadine", "labeler_name": "Aurohealth 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"}