Package 81522-192-09

Brand: allergy relief

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 81522-192-09
Digits Only 8152219209
Product NDC 81522-192
Product ID 81522-192_2fc2551f-18bf-99de-e063-6394a90a6523
Description

1 BOTTLE, PLASTIC in 1 PACKAGE (81522-192-09) / 90 TABLET in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand allergy relief
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Allergy Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2fc2551f-18bf-99de-e063-6394a90a6523", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["276e9767-93c0-5932-e063-6394a90ab2d9"], "manufacturer_name": ["FSA STORE INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 PACKAGE (81522-192-09)  / 90 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "81522-192-09", "marketing_start_date": "20250101"}], "brand_name": "Allergy Relief", "product_id": "81522-192_2fc2551f-18bf-99de-e063-6394a90a6523", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "81522-192", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "FSA STORE INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}