Package 50090-6023-0

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 50090-6023-0
Digits Only 5009060230
Product NDC 50090-6023
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-6023-0)

Marketing

Marketing Status
Marketed Since 2022-06-27
Brand escitalopram
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "77d085a4-81b9-4807-8b43-3b10780c2e77", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["10b25a10-c5e7-479b-a9f5-7eeafd802323"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6023-0)", "package_ndc": "50090-6023-0", "marketing_start_date": "20220627"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6023-1)", "package_ndc": "50090-6023-1", "marketing_start_date": "20220627"}], "brand_name": "Escitalopram", "product_id": "50090-6023_77d085a4-81b9-4807-8b43-3b10780c2e77", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6023", "generic_name": "Escitalopram Oxalate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}