Package 0093-7701-98

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-7701-98
Digits Only 0093770198
Product NDC 0093-7701
Product ID 0093-7701_27746553-05ff-43dd-a541-26bb9a6e9a4c
Description

90 TABLET, FILM COATED in 1 BOTTLE (0093-7701-98)

Marketing

Marketing Status
Marketed Since 2011-09-06
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": "27746553-05ff-43dd-a541-26bb9a6e9a4c", "openfda": {"upc": ["0300937701989"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["4f43d057-cba8-4366-86ba-4be361e4c71f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0093-7701-98)", "package_ndc": "0093-7701-98", "marketing_start_date": "20110906"}], "brand_name": "Levocetirizine Dihydrochloride", "product_id": "0093-7701_27746553-05ff-43dd-a541-26bb9a6e9a4c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0093-7701", "generic_name": "Levocetirizine Dihydrochloride", "labeler_name": "Teva Pharmaceuticals USA, 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"}