Package 68071-5107-9
Brand: levocetirizine dihydrochloride
Generic: levocetirizine dihydrochloridePackage Facts
Identity
Package NDC
68071-5107-9
Digits Only
6807151079
Product NDC
68071-5107
Description
90 TABLET, FILM COATED in 1 BOTTLE (68071-5107-9)
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": "1b469ff6-52ec-a91b-e063-6394a90a3123", "openfda": {"upc": ["0368071510799"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["97a67686-7e94-dd77-e053-2995a90a42c6"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-5107-9)", "package_ndc": "68071-5107-9", "marketing_start_date": "20191118"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "68071-5107_1b469ff6-52ec-a91b-e063-6394a90a3123", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68071-5107", "generic_name": "levocetirizine Dihydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levocetirizine Dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202046", "marketing_category": "ANDA", "marketing_start_date": "20130930", "listing_expiration_date": "20261231"}