Package 57483-230-01
Brand: crcle fexofenadine hydrochloride
Generic: fexofenadine hydrochloridePackage Facts
Identity
Package NDC
57483-230-01
Digits Only
5748323001
Product NDC
57483-230
Description
100 TABLET in 1 CONTAINER (57483-230-01)
Marketing
Marketing Status
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": "100 TABLET in 1 CONTAINER (57483-230-01)", "package_ndc": "57483-230-01", "marketing_start_date": "20230428"}], "brand_name": "Crcle Fexofenadine Hydrochloride", "product_id": "57483-230_f672cd27-4516-4e54-8c4f-8bbdc22dfabd", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57483-230", "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": "60 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20201218", "listing_expiration_date": "20261231"}