Package 68391-955-11
Brand: levocetirizine dihydrochloride
Generic: levocetirizine dihydrochloridePackage Facts
Identity
Package NDC
68391-955-11
Digits Only
6839195511
Product NDC
68391-955
Description
2 BOTTLE in 1 PACKAGE (68391-955-11) / 55 TABLET, COATED in 1 BOTTLE (68391-955-55)
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": "6098f8c4-4502-287f-cd05-06e17d773116", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["0216f644-767c-ae88-f48f-cd29ac1547ed"], "manufacturer_name": ["BJWC (Berkley & Jensen / BJ'S)"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 PACKAGE (68391-955-11) / 55 TABLET, COATED in 1 BOTTLE (68391-955-55)", "package_ndc": "68391-955-11", "marketing_start_date": "20240815"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "68391-955_6098f8c4-4502-287f-cd05-06e17d773116", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68391-955", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "BJWC (Berkley & Jensen / BJ'S)", "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": "20200624", "listing_expiration_date": "20261231"}