Package 31722-569-24

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 31722-569-24
Digits Only 3172256924
Product NDC 31722-569
Product ID 31722-569_1a2252f6-913c-3c7d-e063-6294a90ab194
Description

240 mL in 1 BOTTLE (31722-569-24)

Marketing

Marketing Status
Marketed Since 2012-06-12
Brand escitalopram oxalate
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (1)

Escitalopram Oxalate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1a2252f6-913c-3c7d-e063-6294a90ab194", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["82d793ee-4039-45fc-ac83-4bd5235f00aa"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (31722-569-24)", "package_ndc": "31722-569-24", "marketing_start_date": "20120612"}], "brand_name": "Escitalopram Oxalate", "product_id": "31722-569_1a2252f6-913c-3c7d-e063-6294a90ab194", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "31722-569", "generic_name": "Escitalopram Oxalate", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/5mL"}], "application_number": "ANDA202221", "marketing_category": "ANDA", "marketing_start_date": "20120612", "listing_expiration_date": "20261231"}