Package 83008-065-90

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 83008-065-90
Digits Only 8300806590
Product NDC 83008-065
Product ID 83008-065_8167ad51-fca0-476b-82d7-ca5f131114a7
Description

90 TABLET, FILM COATED in 1 BOTTLE (83008-065-90)

Marketing

Marketing Status
Discontinued 2026-04-08
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

escitalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8167ad51-fca0-476b-82d7-ca5f131114a7", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["9802fe84-45ef-4486-ad4c-6965c1d3bb94"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (83008-065-90)", "package_ndc": "83008-065-90", "marketing_end_date": "20260408", "marketing_start_date": "20240625"}], "brand_name": "escitalopram", "product_id": "83008-065_8167ad51-fca0-476b-82d7-ca5f131114a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "83008-065", "generic_name": "escitalopram", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_end_date": "20260408", "marketing_start_date": "20240625"}