Package 82442-617-26

Brand: up and up childrens allergy

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82442-617-26
Digits Only 8244261726
Product NDC 82442-617
Product ID 82442-617_b0ae7da4-e25b-4ff3-995a-ce3add69c6c2
Description

1 BOTTLE in 1 CARTON (82442-617-26) / 118 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-06-04
Brand up and up childrens allergy
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

up and up childrens allergy ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b0ae7da4-e25b-4ff3-995a-ce3add69c6c2", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["1f37c327-cd4c-4bc1-ae70-713569694e2e"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82442-617-26)  / 118 mL in 1 BOTTLE", "package_ndc": "82442-617-26", "marketing_start_date": "20240604"}], "brand_name": "up and up childrens allergy", "product_id": "82442-617_b0ae7da4-e25b-4ff3-995a-ce3add69c6c2", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "82442-617", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up childrens allergy", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA204226", "marketing_category": "ANDA", "marketing_start_date": "20240604", "listing_expiration_date": "20261231"}