Package 60760-590-90

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 60760-590-90
Digits Only 6076059090
Product NDC 60760-590
Product ID 60760-590_0994403d-1203-49d4-e063-6294a90a6e95
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-590-90)

Marketing

Marketing Status
Marketed Since 2023-10-24
Brand escitalopram
Generic escitalopram oxalate
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": "0994403d-1203-49d4-e063-6294a90a6e95", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["09945404-e4cf-6269-e063-6294a90a5b8d"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-590-90)", "package_ndc": "60760-590-90", "marketing_start_date": "20231024"}], "brand_name": "Escitalopram", "product_id": "60760-590_0994403d-1203-49d4-e063-6294a90a6e95", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-590", "generic_name": "Escitalopram Oxalate", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}