Package 80513-506-01

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 80513-506-01
Digits Only 8051350601
Product NDC 80513-506
Product ID 80513-506_21be7a92-2648-b2bf-e063-6394a90ac580
Description

100 TABLET, FILM COATED in 1 BOTTLE (80513-506-01)

Marketing

Marketing Status
Marketed Since 2024-09-10
Brand fexofenadine hcl
Generic fexofenadine hcl
Sample Package No

Linked Drug Pages (1)

Fexofenadine HCl ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21be7a92-2648-b2bf-e063-6394a90ac580", "openfda": {"upc": ["0380513001382"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["c067b335-79c5-4176-a0b3-bae02a0c23f8"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (80513-506-01)", "package_ndc": "80513-506-01", "marketing_start_date": "20240910"}], "brand_name": "Fexofenadine HCl", "product_id": "80513-506_21be7a92-2648-b2bf-e063-6394a90ac580", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "80513-506", "generic_name": "Fexofenadine HCl", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCl", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_start_date": "20150916", "listing_expiration_date": "20261231"}