Package 43602-473-30

Brand: escitalopram oxalate

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 43602-473-30
Digits Only 4360247330
Product NDC 43602-473
Product ID 43602-473_c891ea0b-ed9d-4e75-a529-2b8a651034d2
Description

30 TABLET in 1 BOTTLE (43602-473-30)

Marketing

Marketing Status
Marketed Since 2025-07-15
Brand escitalopram oxalate
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

ESCITALOPRAM OXALATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c891ea0b-ed9d-4e75-a529-2b8a651034d2", "openfda": {"upc": ["0343602474306", "0343602475303", "0343602474108", "0343602473101", "0343602473309"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["1285841d-d9f8-49c6-9456-bf51c8e37271"], "manufacturer_name": ["Ascent Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (43602-473-10)", "package_ndc": "43602-473-10", "marketing_start_date": "20250715"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (43602-473-30)", "package_ndc": "43602-473-30", "marketing_start_date": "20250715"}], "brand_name": "ESCITALOPRAM OXALATE", "product_id": "43602-473_c891ea0b-ed9d-4e75-a529-2b8a651034d2", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43602-473", "generic_name": "escitalopram", "labeler_name": "Ascent Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESCITALOPRAM OXALATE", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA215177", "marketing_category": "ANDA", "marketing_start_date": "20250715", "listing_expiration_date": "20261231"}