Package 45802-847-78

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 45802-847-78
Digits Only 4580284778
Product NDC 45802-847
Description

1 BOTTLE in 1 CARTON (45802-847-78) / 100 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-01-07
Brand fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e43b561e-d68a-47af-be93-d710f0f77505", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["e43b561e-d68a-47af-be93-d710f0f77505"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (45802-847-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "45802-847-78", "marketing_start_date": "20220107"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "45802-847_e43b561e-d68a-47af-be93-d710f0f77505", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "45802-847", "generic_name": "fexofenadine hydrochloride", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA212971", "marketing_category": "ANDA", "marketing_start_date": "20220107", "listing_expiration_date": "20261231"}