Package 71335-2058-1

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71335-2058-1
Digits Only 7133520581
Product NDC 71335-2058
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-2058-1)

Marketing

Marketing Status
Marketed Since 2022-06-30
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8a8f5825-51d9-466f-88a2-79248f206632", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["43eb9e4f-1a46-46f7-9e9d-43e866963b37"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2058-1)", "package_ndc": "71335-2058-1", "marketing_start_date": "20220630"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2058-2)", "package_ndc": "71335-2058-2", "marketing_start_date": "20250131"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2058-3)", "package_ndc": "71335-2058-3", "marketing_start_date": "20220304"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2058-4)", "package_ndc": "71335-2058-4", "marketing_start_date": "20250131"}], "brand_name": "Escitalopram", "product_id": "71335-2058_8a8f5825-51d9-466f-88a2-79248f206632", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2058", "generic_name": "Escitalopram", "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": "ANDA202389", "marketing_category": "ANDA", "marketing_start_date": "20130305", "listing_expiration_date": "20261231"}