Package 72603-149-01

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 72603-149-01
Digits Only 7260314901
Product NDC 72603-149
Product ID 72603-149_cb888b2f-8092-43a1-8542-a10e2b004369
Description

1000 TABLET, FILM COATED in 1 BOTTLE (72603-149-01)

Marketing

Marketing Status
Marketed Since 2024-01-08
Brand escitalopram oxalate
Generic escitalopram oxalate
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": "cb888b2f-8092-43a1-8542-a10e2b004369", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["81840aec-96fd-4af2-bd10-3f38d068f39a"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72603-149-01)", "package_ndc": "72603-149-01", "marketing_start_date": "20240108"}], "brand_name": "Escitalopram Oxalate", "product_id": "72603-149_cb888b2f-8092-43a1-8542-a10e2b004369", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72603-149", "generic_name": "Escitalopram Oxalate", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA202210", "marketing_category": "ANDA", "marketing_start_date": "20240108", "listing_expiration_date": "20261231"}