Package 68645-520-54

Brand: escitalopram oxalate

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 68645-520-54
Digits Only 6864552054
Product NDC 68645-520
Description

30 TABLET, FILM COATED in 1 BOTTLE (68645-520-54)

Marketing

Marketing Status
Marketed Since 2016-06-16
Brand escitalopram oxalate
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c28cb5c-e64b-9aae-e063-6394a90a9720", "openfda": {"upc": ["0368645519548", "0368645520544"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351250"], "spl_set_id": ["9c68f89b-1d34-4735-9631-817f012935d7"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68645-520-54)", "package_ndc": "68645-520-54", "marketing_start_date": "20160616"}], "brand_name": "Escitalopram Oxalate", "product_id": "68645-520_2c28cb5c-e64b-9aae-e063-6394a90a9720", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68645-520", "generic_name": "Escitalopram", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078604", "marketing_category": "ANDA", "marketing_start_date": "20160616", "listing_expiration_date": "20261231"}