Package 60687-865-01

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 60687-865-01
Digits Only 6068786501
Product NDC 60687-865
Product ID 60687-865_30c946d7-a6ce-e383-e063-6394a90a773e
Description

100 BLISTER PACK in 1 CARTON (60687-865-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-865-11)

Marketing

Marketing Status
Marketed Since 2025-03-20
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": "30c946d7-a6ce-e383-e063-6394a90a773e", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["de803217-6d32-4ef8-afe7-02462f37bf0c"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-865-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-865-11)", "package_ndc": "60687-865-01", "marketing_start_date": "20250320"}], "brand_name": "Escitalopram", "product_id": "60687-865_30c946d7-a6ce-e383-e063-6394a90a773e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60687-865", "generic_name": "Escitalopram", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20250320", "listing_expiration_date": "20261231"}