Package 72789-311-30

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 72789-311-30
Digits Only 7278931130
Product NDC 72789-311
Product ID 72789-311_31f54f70-b635-cb9e-e063-6394a90a329f
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-311-30)

Marketing

Marketing Status
Marketed Since 2023-07-11
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": "31f54f70-b635-cb9e-e063-6394a90a329f", "openfda": {"upc": ["0372789311906"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["517a551a-6f60-4b8d-9341-63a41baff12d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-311-30)", "package_ndc": "72789-311-30", "marketing_start_date": "20230711"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-311-90)", "package_ndc": "72789-311-90", "marketing_start_date": "20230316"}], "brand_name": "Escitalopram", "product_id": "72789-311_31f54f70-b635-cb9e-e063-6394a90a329f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72789-311", "generic_name": "Escitalopram Oxalate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}