Package 31722-659-31

Brand: levocetirizine dihydrochloride

Generic: levocetirizine dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-659-31
Digits Only 3172265931
Product NDC 31722-659
Description

1 BOTTLE in 1 CARTON (31722-659-31) / 148 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-04-01
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": "375cacf2-f8c1-96f1-e063-6394a90ad2df", "openfda": {"upc": ["0331722659314"], "unii": ["SOD6A38AGA"], "rxcui": ["855168"], "spl_set_id": ["dc8adb01-a7ca-490b-b476-8915f1a2e6db"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-659-31)  / 148 mL in 1 BOTTLE", "package_ndc": "31722-659-31", "marketing_start_date": "20190401"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "31722-659_375cacf2-f8c1-96f1-e063-6394a90ad2df", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "31722-659", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "2.5 mg/5mL"}], "application_number": "ANDA210914", "marketing_category": "ANDA", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}