Package 57483-240-02

Brand: crcle fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57483-240-02
Digits Only 5748324002
Product NDC 57483-240
Description

150 TABLET in 1 CONTAINER (57483-240-02)

Marketing

Marketing Status
Marketed Since 2023-04-10
Brand crcle fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f672cd27-4516-4e54-8c4f-8bbdc22dfabd", "openfda": {"upc": ["0357483002466", "0357483002459"], "unii": ["2S068B75ZU"], "rxcui": ["997420", "997501"], "spl_set_id": ["f7784610-7ca5-4489-b391-f2b3f3f6549b"], "manufacturer_name": ["Innovus Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET in 1 CONTAINER (57483-240-02)", "package_ndc": "57483-240-02", "marketing_start_date": "20230410"}], "brand_name": "Crcle Fexofenadine Hydrochloride", "product_id": "57483-240_f672cd27-4516-4e54-8c4f-8bbdc22dfabd", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57483-240", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "Innovus Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Crcle Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20201218", "listing_expiration_date": "20261231"}