Package 80425-0320-2
Brand: escitalopram
Generic: escitalopramPackage Facts
Identity
Package NDC
80425-0320-2
Digits Only
8042503202
Product NDC
80425-0320
Description
60 TABLET, FILM COATED in 1 BOTTLE (80425-0320-2)
Marketing
Marketing Status
Brand
escitalopram
Generic
escitalopram
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a9bf7d3-46db-0dfa-e063-6394a90a76a4", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["f914fec5-4ce7-794d-e053-6294a90a7cc5"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0320-1)", "package_ndc": "80425-0320-1", "marketing_start_date": "20230411"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0320-2)", "package_ndc": "80425-0320-2", "marketing_start_date": "20230411"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0320-3)", "package_ndc": "80425-0320-3", "marketing_start_date": "20230411"}], "brand_name": "Escitalopram", "product_id": "80425-0320_2a9bf7d3-46db-0dfa-e063-6394a90a76a4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "80425-0320", "generic_name": "Escitalopram", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20230411", "listing_expiration_date": "20261231"}