Package 84324-008-01

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84324-008-01
Digits Only 8432400801
Product NDC 84324-008
Product ID 84324-008_16dc8e4f-54e3-4edd-87f8-30d072fabad1
Description

18 TABLET in 1 BOTTLE (84324-008-01)

Marketing

Marketing Status
Marketed Since 2024-07-17
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": "16dc8e4f-54e3-4edd-87f8-30d072fabad1", "openfda": {"upc": ["0384324000060"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["bb47b839-3f49-4818-a62c-b6d2b09b15dc"], "manufacturer_name": ["NUVICARE LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 TABLET in 1 BOTTLE (84324-008-01)", "package_ndc": "84324-008-01", "marketing_start_date": "20240717"}], "brand_name": "FEXOFENADINE HYDROCHLORIDE", "product_id": "84324-008_16dc8e4f-54e3-4edd-87f8-30d072fabad1", "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": "20240717", "listing_expiration_date": "20261231"}