Package 50090-6534-0

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 50090-6534-0
Digits Only 5009065340
Product NDC 50090-6534
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-6534-0)

Marketing

Marketing Status
Marketed Since 2023-06-28
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "488baa4a-7e4b-47f3-94b2-8aa729de9cce", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["2ffc6ec3-830f-46bc-9b3f-7c42cefa39b2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6534-0)", "package_ndc": "50090-6534-0", "marketing_start_date": "20230628"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6534-1)", "package_ndc": "50090-6534-1", "marketing_start_date": "20230628"}], "brand_name": "Escitalopram", "product_id": "50090-6534_488baa4a-7e4b-47f3-94b2-8aa729de9cce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6534", "generic_name": "Escitalopram", "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": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}