Package 50228-202-04

Brand: fexofenadine hcl

Generic: fexofenadine hcl
NDC Package

Package Facts

Identity

Package NDC 50228-202-04
Digits Only 5022820204
Product NDC 50228-202
Product ID 50228-202_2a0b48b8-5955-9ab7-e063-6394a90a6b24
Description

1000 TABLET, FILM COATED in 1 BOTTLE (50228-202-04)

Marketing

Marketing Status
Marketed Since 2014-12-26
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": "2a0b48b8-5955-9ab7-e063-6394a90a6b24", "openfda": {"upc": ["0350228202015", "0350228201032", "0350228202022", "0350228201025", "0350228201018", "0350228202046", "0350228201049", "0350228202039"], "unii": ["2S068B75ZU"], "rxcui": ["997420", "997501"], "spl_set_id": ["b7e9477d-33d9-4463-b8a6-69af5f71ce35"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50228-202-01)", "package_ndc": "50228-202-01", "marketing_start_date": "20141226"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (50228-202-02)", "package_ndc": "50228-202-02", "marketing_start_date": "20141226"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50228-202-03)", "package_ndc": "50228-202-03", "marketing_start_date": "20141226"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (50228-202-04)", "package_ndc": "50228-202-04", "marketing_start_date": "20141226"}], "brand_name": "fexofenadine hcl", "product_id": "50228-202_2a0b48b8-5955-9ab7-e063-6394a90a6b24", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50228-202", "generic_name": "fexofenadine hcl", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "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": "20141226", "listing_expiration_date": "20261231"}