Package 73629-008-03

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 73629-008-03
Digits Only 7362900803
Product NDC 73629-008
Product ID 73629-008_47d41023-701b-09eb-e063-6294a90a7298
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73629-008-03)

Marketing

Marketing Status
Marketed Since 2024-07-27
Brand fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fexofenadine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47d41023-701b-09eb-e063-6294a90a7298", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1e46343f-d6b6-73ba-e063-6394a90acd94"], "manufacturer_name": ["AMZ789 LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73629-008-03)", "package_ndc": "73629-008-03", "marketing_start_date": "20240727"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "73629-008_47d41023-701b-09eb-e063-6294a90a7298", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "73629-008", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "AMZ789 LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20240727", "listing_expiration_date": "20271231"}