Package 0363-5529-55

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-5529-55
Digits Only 0363552955
Product NDC 0363-5529
Product ID 0363-5529_7d5d0782-387a-6951-f77d-da28a0065fef
Description

1 BOTTLE in 1 CARTON (0363-5529-55) / 55 TABLET, COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-03-26
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": "7d5d0782-387a-6951-f77d-da28a0065fef", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["766b8836-74b8-8af7-b900-b813b4fc175b"], "manufacturer_name": ["Walgreens Company"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0363-5529-10)  / 5 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "0363-5529-10", "marketing_start_date": "20180417"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5529-12)  / 120 TABLET, COATED in 1 BOTTLE", "package_ndc": "0363-5529-12", "marketing_start_date": "20210115"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5529-35)  / 35 TABLET, COATED in 1 BOTTLE", "package_ndc": "0363-5529-35", "marketing_start_date": "20180326"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5529-55)  / 55 TABLET, COATED in 1 BOTTLE", "package_ndc": "0363-5529-55", "marketing_start_date": "20180326"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5529-80)  / 80 TABLET, COATED in 1 BOTTLE", "package_ndc": "0363-5529-80", "marketing_start_date": "20180326"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "0363-5529_7d5d0782-387a-6951-f77d-da28a0065fef", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-5529", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Walgreens 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": "20180326", "listing_expiration_date": "20271231"}