Package 82009-035-10

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 82009-035-10
Digits Only 8200903510
Product NDC 82009-035
Product ID 82009-035_8535cead-aff5-4a22-b788-1d5926e02097
Description

1000 TABLET in 1 BOTTLE (82009-035-10)

Marketing

Marketing Status
Marketed Since 2023-03-01
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": "8535cead-aff5-4a22-b788-1d5926e02097", "openfda": {"upc": ["0382009036106"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["d8e22060-4d06-42bf-a881-caaf65ecc3e3"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82009-035-10)", "package_ndc": "82009-035-10", "marketing_start_date": "20230301"}], "brand_name": "escitalopram oxalate", "product_id": "82009-035_8535cead-aff5-4a22-b788-1d5926e02097", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "82009-035", "generic_name": "escitalopram oxalate", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}