Package 69230-328-03

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 69230-328-03
Digits Only 6923032803
Product NDC 69230-328
Description

300 TABLET in 1 BOTTLE (69230-328-03)

Marketing

Marketing Status
Marketed Since 2022-07-31
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": "ef239f47-2514-8b93-e053-2a95a90a4b71", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["1e92f77f-d4ba-4f34-96f9-daf878b4ea6a"], "manufacturer_name": ["Camber Consumer Care Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-328-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "69230-328-01", "marketing_start_date": "20220731"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (69230-328-03)", "package_ndc": "69230-328-03", "marketing_start_date": "20220731"}], "brand_name": "LORATADINE", "product_id": "69230-328_ef239f47-2514-8b93-e053-2a95a90a4b71", "dosage_form": "TABLET", "product_ndc": "69230-328", "generic_name": "LORATADINE", "labeler_name": "Camber Consumer Care Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LORATADINE", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA210722", "marketing_category": "ANDA", "marketing_start_date": "20220731", "listing_expiration_date": "20261231"}