Package 0904-6852-72

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 0904-6852-72
Digits Only 0904685272
Product NDC 0904-6852
Product ID 0904-6852_7c3836c3-7476-49b8-ac03-11718d17c813
Description

1 BOTTLE in 1 CARTON (0904-6852-72) / 300 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-06-04
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": "7c3836c3-7476-49b8-ac03-11718d17c813", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["dee25423-377b-4b94-a4a8-0dfb8f51aaab"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6852-72)  / 300 TABLET in 1 BOTTLE", "package_ndc": "0904-6852-72", "marketing_start_date": "20190604"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6852-89)  / 90 TABLET in 1 BOTTLE", "package_ndc": "0904-6852-89", "marketing_start_date": "20190408"}], "brand_name": "Loratadine", "product_id": "0904-6852_7c3836c3-7476-49b8-ac03-11718d17c813", "dosage_form": "TABLET", "product_ndc": "0904-6852", "generic_name": "Loratadine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076301", "marketing_category": "ANDA", "marketing_start_date": "20050221", "listing_expiration_date": "20261231"}