Package 41167-5803-9

Brand: xyzal

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 41167-5803-9
Digits Only 4116758039
Product NDC 41167-5803
Product ID 41167-5803_87a83f00-5abf-437d-af13-394c22964050
Description

90 TABLET, FILM COATED in 1 BOTTLE (41167-5803-9)

Marketing

Marketing Status
Marketed Since 2017-07-24
Brand xyzal
Generic levocetirizine dihydrochloride
Sample Package No

Linked Drug Pages (1)

Xyzal ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "87a83f00-5abf-437d-af13-394c22964050", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855168", "855170", "855172", "855174"], "spl_set_id": ["1673f7ff-0c7c-4403-86cf-c05eb1475222"], "manufacturer_name": ["Chattem, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (41167-5803-9)", "package_ndc": "41167-5803-9", "marketing_start_date": "20170724"}], "brand_name": "Xyzal", "product_id": "41167-5803_87a83f00-5abf-437d-af13-394c22964050", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "41167-5803", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Chattem, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xyzal", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "NDA022064", "marketing_category": "NDA", "marketing_start_date": "20170724", "listing_expiration_date": "20261231"}