Package 68196-406-20

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 68196-406-20
Digits Only 6819640620
Product NDC 68196-406
Description

2 BOTTLE in 1 CARTON (68196-406-20) / 200 TABLET, COATED in 1 BOTTLE (68196-406-02)

Marketing

Marketing Status
Marketed Since 2023-10-27
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": "35231680-b77b-f06e-11a5-a2107565afd1", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["bb8d38b2-117a-fc6b-4ba0-0bc0188cbcd1"], "manufacturer_name": ["SAM'S WEST INC"]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (68196-406-20)  / 200 TABLET, COATED in 1 BOTTLE (68196-406-02)", "package_ndc": "68196-406-20", "marketing_start_date": "20231027"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "68196-406_35231680-b77b-f06e-11a5-a2107565afd1", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68196-406", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "SAM'S WEST INC", "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": "20200624", "listing_expiration_date": "20271231"}