Package 30142-717-35

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 30142-717-35
Digits Only 3014271735
Product NDC 30142-717
Product ID 30142-717_1a7ae26e-cc7d-442a-8308-48d31a3ade4f
Description

1 BOTTLE in 1 CARTON (30142-717-35) / 35 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-09-30
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": "1a7ae26e-cc7d-442a-8308-48d31a3ade4f", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["e47658af-e0f3-5765-f568-300ba407dc29"], "manufacturer_name": ["KROGER COMPANY"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (30142-717-16)  / 80 TABLET, COATED in 1 BOTTLE (30142-717-80)", "package_ndc": "30142-717-16", "marketing_start_date": "20180930"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-717-35)  / 35 TABLET, COATED in 1 BOTTLE", "package_ndc": "30142-717-35", "marketing_start_date": "20180930"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "30142-717_1a7ae26e-cc7d-442a-8308-48d31a3ade4f", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "30142-717", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210375", "marketing_category": "ANDA", "marketing_start_date": "20180930", "listing_expiration_date": "20271231"}