Package 42543-712-30

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 42543-712-30
Digits Only 4254371230
Product NDC 42543-712
Product ID 42543-712_e0dc4ba0-8ea1-47c3-8bed-427969ca5c15
Description

30 TABLET in 1 BOTTLE (42543-712-30)

Marketing

Marketing Status
Marketed Since 2014-10-27
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": "e0dc4ba0-8ea1-47c3-8bed-427969ca5c15", "openfda": {"upc": ["0342543712904"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["7a2ca8aa-ba0b-45b4-bdb3-651879350130"], "manufacturer_name": ["Vensun Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (42543-712-03)", "package_ndc": "42543-712-03", "marketing_start_date": "20141027"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (42543-712-30)", "package_ndc": "42543-712-30", "marketing_start_date": "20141027"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42543-712-90)", "package_ndc": "42543-712-90", "marketing_start_date": "20141027"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "42543-712_e0dc4ba0-8ea1-47c3-8bed-427969ca5c15", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "42543-712", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Vensun Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203646", "marketing_category": "ANDA", "marketing_start_date": "20141027", "listing_expiration_date": "20261231"}