Package 0904-7426-59

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 0904-7426-59
Digits Only 0904742659
Product NDC 0904-7426
Description

1 BOTTLE in 1 CARTON (0904-7426-59) / 100 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-02-23
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": "8d4a63eb-4112-4312-93c2-05688ea201b3", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["98e41ae1-677a-4583-9a0a-edba29ebbc30"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-7426-46)  / 30 TABLET in 1 BOTTLE", "package_ndc": "0904-7426-46", "marketing_start_date": "20240223"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-7426-59)  / 100 TABLET in 1 BOTTLE", "package_ndc": "0904-7426-59", "marketing_start_date": "20240223"}], "brand_name": "Loratadine", "product_id": "0904-7426_8d4a63eb-4112-4312-93c2-05688ea201b3", "dosage_form": "TABLET", "product_ndc": "0904-7426", "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": "ANDA208314", "marketing_category": "ANDA", "marketing_start_date": "20240223", "listing_expiration_date": "20261231"}