Package 33342-200-07

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 33342-200-07
Digits Only 3334220007
Product NDC 33342-200
Product ID 33342-200_af9c84cc-0f32-4489-a65b-aaa9d93e65e5
Description

30 TABLET, FILM COATED in 1 BOTTLE (33342-200-07)

Marketing

Marketing Status
Marketed Since 2016-01-11
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": "af9c84cc-0f32-4489-a65b-aaa9d93e65e5", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["8a3c06a5-4a9a-4205-8ae7-c58efeb73c58"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (33342-200-07)", "package_ndc": "33342-200-07", "marketing_start_date": "20160111"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-200-10)", "package_ndc": "33342-200-10", "marketing_start_date": "20160111"}], "brand_name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "product_id": "33342-200_af9c84cc-0f32-4489-a65b-aaa9d93e65e5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "33342-200", "generic_name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOCETIRIZINE DIHYDROCHLORIDE", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA205564", "marketing_category": "ANDA", "marketing_start_date": "20160111", "listing_expiration_date": "20261231"}