Package 54257-170-02

Brand: allergy relief

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54257-170-02
Digits Only 5425717002
Product NDC 54257-170
Product ID 54257-170_0e12b912-5db1-bb3e-e063-6394a90aa446
Description

100 TABLET in 1 BOTTLE (54257-170-02)

Marketing

Marketing Status
Marketed Since 2021-03-25
Brand allergy relief
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Allergy Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e12b912-5db1-bb3e-e063-6394a90aa446", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["1f8a2f98-7eba-48df-9589-58587d67ae0e"], "manufacturer_name": ["Magno-Humphries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (54257-170-02)", "package_ndc": "54257-170-02", "marketing_start_date": "20210325"}], "brand_name": "Allergy Relief", "product_id": "54257-170_0e12b912-5db1-bb3e-e063-6394a90aa446", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "54257-170", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "Magno-Humphries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_start_date": "20210325", "listing_expiration_date": "20261231"}