Package 0363-7011-39

Brand: allergy relief

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-7011-39
Digits Only 0363701139
Product NDC 0363-7011
Product ID 0363-7011_0d3aa246-3316-4686-b69c-330ef3b21fcd
Description

1 BOTTLE in 1 CARTON (0363-7011-39) / 30 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-02-08
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": "0d3aa246-3316-4686-b69c-330ef3b21fcd", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["a0738300-7262-4e43-89a6-0d0a60bd14bd"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-7011-39)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-7011-39", "marketing_start_date": "20240208"}], "brand_name": "allergy relief", "product_id": "0363-7011_0d3aa246-3316-4686-b69c-330ef3b21fcd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-7011", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "allergy relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA212971", "marketing_category": "ANDA", "marketing_start_date": "20240208", "listing_expiration_date": "20261231"}