Package 0904-7486-02

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 0904-7486-02
Digits Only 0904748602
Product NDC 0904-7486
Description

30 TABLET, FILM COATED in 1 BOTTLE (0904-7486-02)

Marketing

Marketing Status
Marketed Since 2024-08-20
Brand fexofenadine hcl
Generic fexofenadine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b1390973-4ac1-40c9-b0e1-c7a4d04c0ee4", "openfda": {"upc": ["0309047486021", "0309047486601", "0309047192045", "0309047192601"], "unii": ["2S068B75ZU"], "rxcui": ["997420", "997501"], "spl_set_id": ["107f398c-f296-4190-8234-82556a039e65"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0904-7486-02)", "package_ndc": "0904-7486-02", "marketing_start_date": "20240820"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0904-7486-40)", "package_ndc": "0904-7486-40", "marketing_start_date": "20240820"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0904-7486-60)", "package_ndc": "0904-7486-60", "marketing_start_date": "20240820"}], "brand_name": "fexofenadine hcl", "product_id": "0904-7486_b1390973-4ac1-40c9-b0e1-c7a4d04c0ee4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0904-7486", "generic_name": "fexofenadine hcl", "labeler_name": "Major Pharmaceuticals", "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": "20240820", "listing_expiration_date": "20261231"}