Package 41163-938-35

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 41163-938-35
Digits Only 4116393835
Product NDC 41163-938
Product ID 41163-938_a9a6a71e-7f90-7204-983a-10736fd7814e
Description

1 BOTTLE in 1 CARTON (41163-938-35) / 35 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-12-31
Brand levocetirizine dihydrochloride
Generic levocetirizine dihydrochloride
Sample Package No

Linked Drug Pages (1)

levocetirizine dihydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a9a6a71e-7f90-7204-983a-10736fd7814e", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["5036170d-7eeb-65a8-8473-7d98aeb51ee4"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-938-35)  / 35 TABLET, COATED in 1 BOTTLE", "package_ndc": "41163-938-35", "marketing_start_date": "20181231"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "41163-938_a9a6a71e-7f90-7204-983a-10736fd7814e", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "41163-938", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210375", "marketing_category": "ANDA", "marketing_start_date": "20181231", "listing_expiration_date": "20261231"}