Package 67046-1465-3

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 67046-1465-3
Digits Only 6704614653
Product NDC 67046-1465
Product ID 67046-1465_2d58aaca-22d8-7da2-e063-6394a90af047
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1465-3)

Marketing

Marketing Status
Marketed Since 2025-02-04
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": "2d58aaca-22d8-7da2-e063-6394a90af047", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["2d58c448-4a6c-1b7d-e063-6294a90a7d03"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1465-3)", "package_ndc": "67046-1465-3", "marketing_start_date": "20250204"}], "brand_name": "escitalopram", "product_id": "67046-1465_2d58aaca-22d8-7da2-e063-6394a90af047", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "67046-1465", "generic_name": "escitalopram", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20250204", "listing_expiration_date": "20261231"}