Package 50228-136-30
Brand: levocetirizine dihydrochloride
Generic: levocetirizine dihydrochloridePackage Facts
Identity
Package NDC
50228-136-30
Digits Only
5022813630
Product NDC
50228-136
Description
30 TABLET in 1 BOTTLE (50228-136-30)
Marketing
Marketing Status
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": "9683b976-3b83-43f0-959c-5f238b84602e", "openfda": {"upc": ["0350228136907", "0350228136303"], "unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["bd7fe481-dfe7-4dfd-aa05-6e2318a9234e"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-136-10)", "package_ndc": "50228-136-10", "marketing_start_date": "20140909"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-136-30)", "package_ndc": "50228-136-30", "marketing_start_date": "20140909"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50228-136-90)", "package_ndc": "50228-136-90", "marketing_start_date": "20140909"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "50228-136_9683b976-3b83-43f0-959c-5f238b84602e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50228-136", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203646", "marketing_category": "ANDA", "marketing_start_date": "20140909", "listing_expiration_date": "20261231"}