Package 50090-7200-0
Brand: escitalopram oxalate
Generic: escitalopram oxalatePackage Facts
Identity
Package NDC
50090-7200-0
Digits Only
5009072000
Product NDC
50090-7200
Description
30 TABLET, FILM COATED in 1 BOTTLE (50090-7200-0)
Marketing
Marketing Status
Brand
escitalopram oxalate
Generic
escitalopram oxalate
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c54a04b2-8d7d-4a25-8f53-aa075eea042b", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["c980262b-31f0-46df-902d-e593e1557fef"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7200-0)", "package_ndc": "50090-7200-0", "marketing_start_date": "20240730"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7200-1)", "package_ndc": "50090-7200-1", "marketing_start_date": "20240730"}], "brand_name": "Escitalopram Oxalate", "product_id": "50090-7200_c54a04b2-8d7d-4a25-8f53-aa075eea042b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7200", "generic_name": "Escitalopram Oxalate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/21"}], "application_number": "ANDA202210", "marketing_category": "ANDA", "marketing_start_date": "20240108", "listing_expiration_date": "20261231"}