Package 82982-065-60

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 82982-065-60
Digits Only 8298206560
Product NDC 82982-065
Product ID 82982-065_198ba216-39a7-3d98-e063-6394a90a9f0b
Description

60 TABLET in 1 BOTTLE (82982-065-60)

Marketing

Marketing Status
Discontinued 2026-07-31
Brand escitalopram oxalate
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (1)

escitalopram oxalate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "198ba216-39a7-3d98-e063-6394a90a9f0b", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["faa48e9c-a34c-c745-e053-6294a90a9b21"], "manufacturer_name": ["Pharmasource Meds, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (82982-065-60)", "package_ndc": "82982-065-60", "marketing_end_date": "20260731", "marketing_start_date": "20230501"}], "brand_name": "escitalopram oxalate", "product_id": "82982-065_198ba216-39a7-3d98-e063-6394a90a9f0b", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "82982-065", "generic_name": "escitalopram oxalate", "labeler_name": "Pharmasource Meds, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20230501"}