Package 43063-479-30

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-479-30
Digits Only 4306347930
Product NDC 43063-479
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-479-30)

Marketing

Marketing Status
Marketed Since 2013-10-30
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": "3ed97d6e-d710-dd18-e063-6294a90ac4ae", "openfda": {"upc": ["0343063479308"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["344ba2d6-4e17-4cef-bd7b-248fbb1af3b6"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-479-30)", "package_ndc": "43063-479-30", "marketing_start_date": "20131030"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "43063-479_3ed97d6e-d710-dd18-e063-6294a90ac4ae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "43063-479", "generic_name": "Levocetirizine Dihydrochloride", "labeler_name": "PD-Rx 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"}