Package 65862-248-24

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 65862-248-24
Digits Only 6586224824
Product NDC 65862-248
Product ID 65862-248_5ce05169-cc04-44be-9e45-9e89d244123b
Description

240 mL in 1 BOTTLE (65862-248-24)

Marketing

Marketing Status
Marketed Since 2012-04-03
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": "5ce05169-cc04-44be-9e45-9e89d244123b", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["ba60c357-8e61-4a3d-b1dc-25602dbbfc2a"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (65862-248-24)", "package_ndc": "65862-248-24", "marketing_start_date": "20120403"}], "brand_name": "Escitalopram Oxalate", "product_id": "65862-248_5ce05169-cc04-44be-9e45-9e89d244123b", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-248", "generic_name": "Escitalopram Oxalate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/5mL"}], "application_number": "ANDA079062", "marketing_category": "ANDA", "marketing_start_date": "20120403", "listing_expiration_date": "20261231"}