Package 0363-6231-24

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 0363-6231-24
Digits Only 0363623124
Product NDC 0363-6231
Description

24 TABLET in 1 BOTTLE (0363-6231-24)

Marketing

Marketing Status
Marketed Since 2024-07-23
Brand fexofenadine hcl
Generic fexofenadine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4654a188-db7a-2770-e063-6394a90a278e", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["0eaf28a5-f8dd-3888-e063-6394a90a8cc6"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET in 1 BOTTLE (0363-6231-24)", "package_ndc": "0363-6231-24", "marketing_start_date": "20240723"}], "brand_name": "Fexofenadine HCL", "product_id": "0363-6231_4654a188-db7a-2770-e063-6394a90a278e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-6231", "generic_name": "Fexofenadine HCL", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCL", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20240723", "listing_expiration_date": "20261231"}