Package 68071-3726-9

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3726-9
Digits Only 6807137269
Product NDC 68071-3726
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-3726-9)

Marketing

Marketing Status
Marketed Since 2024-11-22
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": "27878da9-3e05-df72-e063-6394a90a378b", "openfda": {"upc": ["0368071372694"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["2787aaa2-5209-f7d5-e063-6294a90a7103"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3726-9)", "package_ndc": "68071-3726-9", "marketing_start_date": "20241122"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "68071-3726_27878da9-3e05-df72-e063-6394a90a378b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68071-3726", "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": "ANDA090199", "marketing_category": "ANDA", "marketing_start_date": "20110906", "listing_expiration_date": "20261231"}