Package 69367-238-09

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-238-09
Digits Only 6936723809
Product NDC 69367-238
Product ID 69367-238_173f9840-08fa-4972-a624-0c716356d7ee
Description

90 TABLET in 1 BOTTLE, PLASTIC (69367-238-09)

Marketing

Marketing Status
Marketed Since 2019-09-19
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": "173f9840-08fa-4972-a624-0c716356d7ee", "openfda": {"upc": ["0369367238090"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["85dcd6c0-7fb2-40b3-b07f-93bab169011d"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (69367-238-09)", "package_ndc": "69367-238-09", "marketing_start_date": "20190919"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "69367-238_173f9840-08fa-4972-a624-0c716356d7ee", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69367-238", "generic_name": "Levocetirizine Dihydrochloride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levocetirizine Dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203646", "marketing_category": "ANDA", "marketing_start_date": "20190919", "listing_expiration_date": "20261231"}