Package 76420-723-30
Brand: escitalopram
Generic: escitalopram oxalatePackage Facts
Identity
Package NDC
76420-723-30
Digits Only
7642072330
Product NDC
76420-723
Description
30 TABLET, FILM COATED in 1 BOTTLE (76420-723-30)
Marketing
Marketing Status
Brand
escitalopram
Generic
escitalopram oxalate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ac15baa-6fcc-476b-e063-6294a90a2a89", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["2957a003-7714-4e16-aeca-623fd6c5d702"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-723-01)", "package_ndc": "76420-723-01", "marketing_start_date": "20240506"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76420-723-05)", "package_ndc": "76420-723-05", "marketing_start_date": "20240506"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (76420-723-10)", "package_ndc": "76420-723-10", "marketing_start_date": "20240506"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-723-30)", "package_ndc": "76420-723-30", "marketing_start_date": "20240506"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-723-60)", "package_ndc": "76420-723-60", "marketing_start_date": "20240506"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-723-90)", "package_ndc": "76420-723-90", "marketing_start_date": "20240506"}], "brand_name": "Escitalopram", "product_id": "76420-723_4ac15baa-6fcc-476b-e063-6294a90a2a89", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "76420-723", "generic_name": "Escitalopram Oxalate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20271231"}