Package 72090-010-01

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72090-010-01
Digits Only 7209001001
Product NDC 72090-010
Product ID 72090-010_2aa6e396-3103-48d1-bcd7-43b140549307
Description

90 TABLET in 1 BOTTLE (72090-010-01)

Marketing

Marketing Status
Marketed Since 2023-12-07
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": "2aa6e396-3103-48d1-bcd7-43b140549307", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["d7fe71e4-aada-40f5-86a8-bf0d7eb9b851"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72090-010-01)", "package_ndc": "72090-010-01", "marketing_start_date": "20231207"}], "brand_name": "FEXOFENADINE HYDROCHLORIDE", "product_id": "72090-010_2aa6e396-3103-48d1-bcd7-43b140549307", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72090-010", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "Pioneer Life Sciences, 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": "20231207", "listing_expiration_date": "20261231"}