Package 71335-1952-2
Brand: levocetirizine dihydrochloride
Generic: levocetirizine dihydrochloridePackage Facts
Identity
Package NDC
71335-1952-2
Digits Only
7133519522
Product NDC
71335-1952
Description
90 TABLET in 1 BOTTLE (71335-1952-2)
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": "f1247810-d7f4-4018-977c-25f8e62f3f84", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["8274ca80-e7d3-4f4f-9901-cc5c589b4fef"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1952-1)", "package_ndc": "71335-1952-1", "marketing_start_date": "20210930"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1952-2)", "package_ndc": "71335-1952-2", "marketing_start_date": "20210930"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1952-3)", "package_ndc": "71335-1952-3", "marketing_start_date": "20210930"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1952-4)", "package_ndc": "71335-1952-4", "marketing_start_date": "20210930"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "71335-1952_f1247810-d7f4-4018-977c-25f8e62f3f84", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71335-1952", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}