Package 71335-0418-2
Brand: levocetirizine dihydrochloride
Generic: levocetirizine dihydrochloridePackage Facts
Identity
Package NDC
71335-0418-2
Digits Only
7133504182
Product NDC
71335-0418
Description
90 TABLET, FILM COATED in 1 BOTTLE (71335-0418-2)
Marketing
Marketing Status
Brand
levocetirizine dihydrochloride
Generic
levocetirizine dihydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30c06d79-0809-46a9-a520-2f92cbeb4797", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["1b593c65-2866-45d9-9c94-ac181f4cbc51"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0418-1)", "package_ndc": "71335-0418-1", "marketing_start_date": "20170830"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0418-2)", "package_ndc": "71335-0418-2", "marketing_start_date": "20170830"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-0418-3)", "package_ndc": "71335-0418-3", "marketing_start_date": "20170830"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0418-4)", "package_ndc": "71335-0418-4", "marketing_start_date": "20170830"}], "brand_name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "product_id": "71335-0418_30c06d79-0809-46a9-a520-2f92cbeb4797", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71335-0418", "generic_name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOCETIRIZINE DIHYDROCHLORIDE", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA205564", "marketing_category": "ANDA", "marketing_start_date": "20160111", "listing_expiration_date": "20261231"}