Package 84324-008-02

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84324-008-02
Digits Only 8432400802
Product NDC 84324-008
Product ID 84324-008_5788217f-a09d-407f-a749-d7fed955ea1b
Description

4 TABLET in 1 BLISTER PACK (84324-008-02)

Marketing

Marketing Status
Marketed Since 2025-06-09
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": "5788217f-a09d-407f-a749-d7fed955ea1b", "openfda": {"upc": ["0384324000206"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["ec55732c-a3db-4445-a06d-0f98b21ed134"], "manufacturer_name": ["NUVICARE LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BLISTER PACK (84324-008-02)", "package_ndc": "84324-008-02", "marketing_start_date": "20250609"}], "brand_name": "FEXOFENADINE HYDROCHLORIDE", "product_id": "84324-008_5788217f-a09d-407f-a749-d7fed955ea1b", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "84324-008", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "NUVICARE LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FEXOFENADINE HYDROCHLORIDE", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA210137", "marketing_category": "ANDA", "marketing_start_date": "20250609", "listing_expiration_date": "20261231"}