Package 33342-053-28

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 33342-053-28
Digits Only 3334205328
Product NDC 33342-053
Product ID 33342-053_6dea1a7d-7262-4d3e-9c9e-1db9c8587066
Description

240 mL in 1 BOTTLE (33342-053-28)

Marketing

Marketing Status
Marketed Since 2016-03-31
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": "6dea1a7d-7262-4d3e-9c9e-1db9c8587066", "openfda": {"upc": ["0333342053282"], "unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["4d5c3142-b850-49b9-9f5c-81fe15ea7bfb"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (33342-053-28)", "package_ndc": "33342-053-28", "marketing_start_date": "20160331"}], "brand_name": "escitalopram", "product_id": "33342-053_6dea1a7d-7262-4d3e-9c9e-1db9c8587066", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "33342-053", "generic_name": "escitalopram", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/5mL"}], "application_number": "ANDA202754", "marketing_category": "ANDA", "marketing_start_date": "20160331", "listing_expiration_date": "20261231"}