Package 79481-7660-4

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 79481-7660-4
Digits Only 7948176604
Product NDC 79481-7660
Product ID 79481-7660_4651bada-437a-80ca-e063-6294a90aa378
Description

45 TABLET in 1 BOTTLE (79481-7660-4)

Marketing

Marketing Status
Marketed Since 2024-09-09
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": "4651bada-437a-80ca-e063-6294a90aa378", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["181c7faf-b27d-0a2d-e063-6294a90ad1f4"], "manufacturer_name": ["Meijer"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET in 1 BOTTLE (79481-7660-4)", "package_ndc": "79481-7660-4", "marketing_start_date": "20240909"}], "brand_name": "Fexofenadine HCL", "product_id": "79481-7660_4651bada-437a-80ca-e063-6294a90aa378", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "79481-7660", "generic_name": "Fexofenadine HCL", "labeler_name": "Meijer", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCL", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20240909", "listing_expiration_date": "20261231"}