Package 68071-5107-9

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package 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
Marketed Since 2019-11-18
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"}