Package 71335-9687-2

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 71335-9687-2
Digits Only 7133596872
Product NDC 71335-9687
Product ID 71335-9687_fada57d1-668f-4890-9873-f48716441db1
Description

60 TABLET, FILM COATED in 1 BOTTLE (71335-9687-2)

Marketing

Marketing Status
Marketed Since 2023-04-04
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": "fada57d1-668f-4890-9873-f48716441db1", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["ee5963ad-3b53-48e5-b7a9-b13af5740ef1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-9687-1)", "package_ndc": "71335-9687-1", "marketing_start_date": "20230622"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-9687-2)", "package_ndc": "71335-9687-2", "marketing_start_date": "20230404"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-9687-3)", "package_ndc": "71335-9687-3", "marketing_start_date": "20230710"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-9687-4)", "package_ndc": "71335-9687-4", "marketing_start_date": "20241101"}], "brand_name": "Escitalopram", "product_id": "71335-9687_fada57d1-668f-4890-9873-f48716441db1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-9687", "generic_name": "Escitalopram Oxalate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}