Package 71399-8659-5

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 71399-8659-5
Digits Only 7139986595
Product NDC 71399-8659
Product ID 71399-8659_48c50815-5149-7bba-e063-6294a90a714d
Description

500 TABLET, FILM COATED in 1 BOTTLE (71399-8659-5)

Marketing

Marketing Status
Marketed Since 2024-02-02
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": "48c50815-5149-7bba-e063-6294a90a714d", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997501"], "spl_set_id": ["fe67f0f1-c6f1-424e-8226-19176de79945"], "manufacturer_name": ["AKRON PHARMA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71399-8659-1)", "package_ndc": "71399-8659-1", "marketing_start_date": "20211101"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71399-8659-5)", "package_ndc": "71399-8659-5", "marketing_start_date": "20240202"}], "brand_name": "fexofenadine hcl", "product_id": "71399-8659_48c50815-5149-7bba-e063-6294a90a714d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71399-8659", "generic_name": "fexofenadine hcl", "labeler_name": "AKRON PHARMA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "fexofenadine hcl", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_start_date": "20141226", "listing_expiration_date": "20271231"}