Package 82442-207-26

Brand: up and up childrens allergy

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 82442-207-26
Digits Only 8244220726
Product NDC 82442-207
Description

1 BOTTLE in 1 CARTON (82442-207-26) / 120 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-07-31
Brand up and up childrens allergy
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36a8b979-6403-4545-82e0-d3bccdd2654e", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["692783"], "spl_set_id": ["a9f6ae02-cf29-4111-99e7-7e6b1ecb88f0"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82442-207-26)  / 120 mL in 1 BOTTLE", "package_ndc": "82442-207-26", "marketing_start_date": "20240731"}], "brand_name": "UP AND UP CHILDRENS ALLERGY", "product_id": "82442-207_36a8b979-6403-4545-82e0-d3bccdd2654e", "dosage_form": "SOLUTION", "product_ndc": "82442-207", "generic_name": "Loratadine", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UP AND UP CHILDRENS ALLERGY", "active_ingredients": [{"name": "LORATADINE", "strength": "5 mg/5mL"}], "application_number": "ANDA075728", "marketing_category": "ANDA", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}