Package 82725-3002-1

Brand: cabinet allergy relief fexofenadine

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82725-3002-1
Digits Only 8272530021
Product NDC 82725-3002
Description

100 TABLET in 1 BOTTLE (82725-3002-1)

Marketing

Marketing Status
Discontinued 2027-09-01
Brand cabinet allergy relief fexofenadine
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42da3220-d6d7-3f7f-e063-6394a90a95ef", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["9ed710e1-47f4-4d04-a509-12c8c97c192c"], "manufacturer_name": ["Cabinet Health P.B.C."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82725-3002-1)", "package_ndc": "82725-3002-1", "marketing_end_date": "20270901", "marketing_start_date": "20250101"}], "brand_name": "Cabinet Allergy Relief Fexofenadine", "product_id": "82725-3002_42da3220-d6d7-3f7f-e063-6394a90a95ef", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82725-3002", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "Cabinet Health P.B.C.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cabinet Allergy Relief Fexofenadine", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_end_date": "20270901", "marketing_start_date": "20250101"}