Package 58602-844-60

Brand: fexofenadine hydrochloride and pseudoephedrine hydrochloride

Generic: fexofenadine hydrochloride and pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 58602-844-60
Digits Only 5860284460
Product NDC 58602-844
Description

1 BLISTER PACK in 1 CARTON (58602-844-60) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-04-17
Brand fexofenadine hydrochloride and pseudoephedrine hydrochloride
Generic fexofenadine hydrochloride and pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bced0a2e-047e-456e-bbd2-495e83bf07ee", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997415"], "spl_set_id": ["bced0a2e-047e-456e-bbd2-495e83bf07ee"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (58602-844-60)  / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-844-60", "marketing_start_date": "20250417"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (58602-844-66)  / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-844-66", "marketing_start_date": "20250417"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (58602-844-85)  / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-844-85", "marketing_start_date": "20250417"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "58602-844_bced0a2e-047e-456e-bbd2-495e83bf07ee", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "58602-844", "generic_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "ANDA215232", "marketing_category": "ANDA", "marketing_start_date": "20250417", "listing_expiration_date": "20261231"}