Package 71205-210-30

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-210-30
Digits Only 7120521030
Product NDC 71205-210
Product ID 71205-210_1913d2a6-6558-4d2b-bc1e-54cdef6623eb
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-210-30)

Marketing

Marketing Status
Marketed Since 2019-01-01
Brand levocetirizine dihydrochloride
Generic levocetirizine dihydrochloride
Sample Package No

Linked Drug Pages (1)

Levocetirizine Dihydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1913d2a6-6558-4d2b-bc1e-54cdef6623eb", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["f10cfe9a-1884-4a65-b827-8fd781fb75c4"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-210-30)", "package_ndc": "71205-210-30", "marketing_start_date": "20190101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-210-60)", "package_ndc": "71205-210-60", "marketing_start_date": "20190101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-210-90)", "package_ndc": "71205-210-90", "marketing_start_date": "20190101"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "71205-210_1913d2a6-6558-4d2b-bc1e-54cdef6623eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71205-210", "generic_name": "levocetirizine Dihydrochloride", "labeler_name": "Proficient Rx LP", "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"}