Package 71205-739-90

Brand: fexofenadine hydrochloride

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-739-90
Digits Only 7120573990
Product NDC 71205-739
Product ID 71205-739_4a9b4b7f-0441-44d3-86c7-2542ef4b119a
Description

90 TABLET, FILM COATED in 1 BOTTLE (71205-739-90)

Marketing

Marketing Status
Marketed Since 2022-12-28
Brand fexofenadine hydrochloride
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fexofenadine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a9b4b7f-0441-44d3-86c7-2542ef4b119a", "openfda": {"upc": ["0371205739607"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["4a9b4b7f-0441-44d3-86c7-2542ef4b119a"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-739-30)", "package_ndc": "71205-739-30", "marketing_start_date": "20221228"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-739-60)", "package_ndc": "71205-739-60", "marketing_start_date": "20221228"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-739-90)", "package_ndc": "71205-739-90", "marketing_start_date": "20221228"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "71205-739_4a9b4b7f-0441-44d3-86c7-2542ef4b119a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71205-739", "generic_name": "fexofenadine hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA212971", "marketing_category": "ANDA", "marketing_start_date": "20220107", "listing_expiration_date": "20261231"}