Package 80425-0375-3

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 80425-0375-3
Digits Only 8042503753
Product NDC 80425-0375
Product ID 80425-0375_14077a5d-dd96-3661-e063-6294a90a484a
Description

90 TABLET, FILM COATED in 1 BOTTLE (80425-0375-3)

Marketing

Marketing Status
Marketed Since 2024-03-13
Brand escitalopram
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (1)

Escitalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "14077a5d-dd96-3661-e063-6294a90a484a", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["138f8703-2f13-6d07-e063-6394a90a4413"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0375-1)", "package_ndc": "80425-0375-1", "marketing_start_date": "20240313"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0375-2)", "package_ndc": "80425-0375-2", "marketing_start_date": "20240313"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0375-3)", "package_ndc": "80425-0375-3", "marketing_start_date": "20240313"}], "brand_name": "Escitalopram", "product_id": "80425-0375_14077a5d-dd96-3661-e063-6294a90a484a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "80425-0375", "generic_name": "Escitalopram Oxalate", "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": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20240313", "listing_expiration_date": "20261231"}