Package 50090-6496-0

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 50090-6496-0
Digits Only 5009064960
Product NDC 50090-6496
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-6496-0)

Marketing

Marketing Status
Marketed Since 2023-05-24
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": "3e7b0da2-d2e3-491d-9c2a-f1b0ad7554af", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["b85ef018-0217-4ddf-885d-206acc0a5f84"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6496-0)", "package_ndc": "50090-6496-0", "marketing_start_date": "20230524"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6496-1)", "package_ndc": "50090-6496-1", "marketing_start_date": "20230526"}], "brand_name": "Escitalopram", "product_id": "50090-6496_3e7b0da2-d2e3-491d-9c2a-f1b0ad7554af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6496", "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": "10 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}