Package 58602-831-17

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 58602-831-17
Digits Only 5860283117
Product NDC 58602-831
Description

1 BOTTLE in 1 CARTON (58602-831-17) / 45 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-04-16
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": "de409efa-eff4-47fb-a6c6-a22be0587553", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["839e2e03-9ebb-4a44-b753-fb174bd36115"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-831-17)  / 45 TABLET in 1 BOTTLE", "package_ndc": "58602-831-17", "marketing_start_date": "20180416"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-831-19)  / 90 TABLET in 1 BOTTLE", "package_ndc": "58602-831-19", "marketing_start_date": "20180416"}], "brand_name": "Loratadine", "product_id": "58602-831_de409efa-eff4-47fb-a6c6-a22be0587553", "dosage_form": "TABLET", "product_ndc": "58602-831", "generic_name": "Loratadine", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA208314", "marketing_category": "ANDA", "marketing_start_date": "20180416", "listing_expiration_date": "20261231"}