Package 71335-1241-2

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71335-1241-2
Digits Only 7133512412
Product NDC 71335-1241
Description

60 TABLET, FILM COATED in 1 BOTTLE (71335-1241-2)

Marketing

Marketing Status
Marketed Since 2024-04-03
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": "f7726916-4977-46dc-bb0d-4de18473548b", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["20281fe6-7db9-4b33-8418-b25e6a5404ca"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1241-1)", "package_ndc": "71335-1241-1", "marketing_start_date": "20190702"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1241-2)", "package_ndc": "71335-1241-2", "marketing_start_date": "20240403"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1241-3)", "package_ndc": "71335-1241-3", "marketing_start_date": "20190604"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1241-4)", "package_ndc": "71335-1241-4", "marketing_start_date": "20240403"}], "brand_name": "Escitalopram", "product_id": "71335-1241_f7726916-4977-46dc-bb0d-4de18473548b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-1241", "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": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}