Package 72090-010-99

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72090-010-99
Digits Only 7209001099
Product NDC 72090-010
Product ID 72090-010_3fd79863-077e-4c9c-958d-91f709c6d033
Description

1000 TABLET in 1 BOTTLE (72090-010-99)

Marketing

Marketing Status
Marketed Since 2023-08-11
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": "3fd79863-077e-4c9c-958d-91f709c6d033", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["d3b6f04c-60d6-4ac3-9fb2-19eeb80f00a5"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72090-010-99)", "package_ndc": "72090-010-99", "marketing_start_date": "20230811"}], "brand_name": "FEXOFENADINE HYDROCHLORIDE", "product_id": "72090-010_3fd79863-077e-4c9c-958d-91f709c6d033", "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": "20230811", "listing_expiration_date": "20261231"}