Package 82442-300-72

Brand: up and up non drowsy allergy relief

Generic: fexofenadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82442-300-72
Digits Only 8244230072
Product NDC 82442-300
Description

1 BOTTLE in 1 CARTON (82442-300-72) / 60 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-03-04
Brand up and up non drowsy allergy relief
Generic fexofenadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bd226cd0-be8c-4db9-878f-5c84f6016dcc", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["d251b0a6-bc31-45b6-aaa8-f50f8336d959"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82442-300-72)  / 60 TABLET, COATED in 1 BOTTLE", "package_ndc": "82442-300-72", "marketing_start_date": "20240304"}], "brand_name": "up and up non drowsy allergy relief", "product_id": "82442-300_bd226cd0-be8c-4db9-878f-5c84f6016dcc", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82442-300", "generic_name": "fexofenadine hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up non drowsy allergy relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA212971", "marketing_category": "ANDA", "marketing_start_date": "20240304", "listing_expiration_date": "20261231"}