Package 68001-592-08

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 68001-592-08
Digits Only 6800159208
Product NDC 68001-592
Product ID 68001-592_3f619ebc-6f45-5959-e063-6294a90a61af
Description

1000 TABLET, FILM COATED in 1 BOTTLE (68001-592-08)

Marketing

Marketing Status
Marketed Since 2023-12-14
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": "3f619ebc-6f45-5959-e063-6294a90a61af", "openfda": {"upc": ["0368001593007", "0368001591003", "0368001592000"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["d31c02d0-81d9-4aa4-bde9-52135aa5a66d"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68001-592-00)", "package_ndc": "68001-592-00", "marketing_start_date": "20231214"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68001-592-08)", "package_ndc": "68001-592-08", "marketing_start_date": "20231214"}], "brand_name": "Escitalopram", "product_id": "68001-592_3f619ebc-6f45-5959-e063-6294a90a61af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68001-592", "generic_name": "Escitalopram", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20231214", "listing_expiration_date": "20261231"}