Package 82442-300-72
Brand: up and up non drowsy allergy relief
Generic: fexofenadine hydrochloridePackage 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
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"}