Package 51316-768-06

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 51316-768-06
Digits Only 5131676806
Product NDC 51316-768
Product ID 51316-768_46543162-60f8-aefc-e063-6394a90ac56e
Description

60 TABLET in 1 BOTTLE (51316-768-06)

Marketing

Marketing Status
Marketed Since 2024-01-01
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": "46543162-60f8-aefc-e063-6394a90ac56e", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["013ef192-5184-b720-e063-6394a90a98c4"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (51316-768-06)", "package_ndc": "51316-768-06", "marketing_start_date": "20240101"}], "brand_name": "Fexofenadine HCL", "product_id": "51316-768_46543162-60f8-aefc-e063-6394a90ac56e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51316-768", "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": "20240101", "listing_expiration_date": "20261231"}