Package 85237-0190-3

Brand: allegra allergy 24 hour

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 85237-0190-3
Digits Only 8523701903
Product NDC 85237-0190
Description

1 BLISTER PACK in 1 POUCH (85237-0190-3) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-02-18
Brand allegra allergy 24 hour
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2de81a41-8489-7e39-e063-6294a90a394b", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420", "997422"], "spl_set_id": ["2de81a41-8488-7e39-e063-6294a90a394b"], "manufacturer_name": ["Select Consumer Group"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 POUCH (85237-0190-3)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "85237-0190-3", "marketing_start_date": "20250218"}], "brand_name": "Allegra Allergy 24 hour", "product_id": "85237-0190_2de81a41-8489-7e39-e063-6294a90a394b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "85237-0190", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Select Consumer Group", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allegra Allergy 24 hour", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250218", "listing_expiration_date": "20261231"}