Package 16571-757-10

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 16571-757-10
Digits Only 1657175710
Product NDC 16571-757
Product ID 16571-757_9929f3a5-d78b-4d99-bf87-d2693a9ac47e
Description

1000 TABLET, FILM COATED in 1 BOTTLE (16571-757-10)

Marketing

Marketing Status
Marketed Since 2023-06-10
Brand escitalopram
Generic escitalopram
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": "9929f3a5-d78b-4d99-bf87-d2693a9ac47e", "openfda": {"upc": ["0316571756018"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["ccbe97b5-da68-4fff-929a-240dd705fe6f"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16571-757-01)", "package_ndc": "16571-757-01", "marketing_start_date": "20230610"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16571-757-10)", "package_ndc": "16571-757-10", "marketing_start_date": "20230610"}], "brand_name": "escitalopram", "product_id": "16571-757_9929f3a5-d78b-4d99-bf87-d2693a9ac47e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16571-757", "generic_name": "escitalopram", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}