Package 51316-767-03

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 51316-767-03
Digits Only 5131676703
Product NDC 51316-767
Product ID 51316-767_46540fb6-3247-8ddd-e063-6394a90ae0cb
Description

30 TABLET in 1 BOTTLE (51316-767-03)

Marketing

Marketing Status
Marketed Since 2024-03-27
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": "46540fb6-3247-8ddd-e063-6394a90ae0cb", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["00ef8467-30a0-7579-e063-6294a90a75af"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (51316-767-03)", "package_ndc": "51316-767-03", "marketing_start_date": "20240327"}], "brand_name": "Fexofenadine HCL", "product_id": "51316-767_46540fb6-3247-8ddd-e063-6394a90ae0cb", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51316-767", "generic_name": "Fexofenadine HCL", "labeler_name": "CVS", "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": "20240327", "listing_expiration_date": "20261231"}