Package 16571-769-24

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 16571-769-24
Digits Only 1657176924
Product NDC 16571-769
Product ID 16571-769_abf4fee5-eae0-4b5c-8b7d-7d055d36e530
Description

240 mL in 1 BOTTLE (16571-769-24)

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": "abf4fee5-eae0-4b5c-8b7d-7d055d36e530", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["79fddc2d-2dc2-444f-8fd3-0337090ee744"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (16571-769-24)", "package_ndc": "16571-769-24", "marketing_start_date": "20120403"}], "brand_name": "Escitalopram Oxalate", "product_id": "16571-769_abf4fee5-eae0-4b5c-8b7d-7d055d36e530", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16571-769", "generic_name": "Escitalopram Oxalate", "labeler_name": "Rising Pharma Holdings, Inc.", "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"}