Package 65162-019-09
Brand: escitalopram oxalate
Generic: escitalopram oxalatePackage Facts
Identity
Package NDC
65162-019-09
Digits Only
6516201909
Product NDC
65162-019
Description
90 TABLET, FILM COATED in 1 BOTTLE (65162-019-09)
Marketing
Marketing Status
Brand
escitalopram oxalate
Generic
escitalopram oxalate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "058fe58a-fa86-459a-b79a-ac337913bc7e", "openfda": {"upc": ["0365162021035", "0365162020038"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["8704d062-fa91-4224-9dec-41664d20ee6b"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65162-019-03)", "package_ndc": "65162-019-03", "marketing_start_date": "20170517"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65162-019-09)", "package_ndc": "65162-019-09", "marketing_start_date": "20170517"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65162-019-11)", "package_ndc": "65162-019-11", "marketing_start_date": "20170517"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65162-019-50)", "package_ndc": "65162-019-50", "marketing_start_date": "20170517"}], "brand_name": "Escitalopram Oxalate", "product_id": "65162-019_058fe58a-fa86-459a-b79a-ac337913bc7e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65162-019", "generic_name": "Escitalopram Oxalate", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA205619", "marketing_category": "ANDA", "marketing_start_date": "20170517", "listing_expiration_date": "20261231"}