Package 33342-038-15

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 33342-038-15
Digits Only 3334203815
Product NDC 33342-038
Description

500 TABLET, FILM COATED in 1 BOTTLE (33342-038-15)

Marketing

Marketing Status
Marketed Since 2015-09-09
Brand escitalopram oxalate
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "53210109-53db-4d08-8ea4-be60e5597caf", "openfda": {"upc": ["0333342036155", "0333342037152", "0333342037114", "0333342038159", "0333342038111", "0333342036117"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["24b43cb4-1a26-44a2-b1d8-a40239eb5c7c"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (33342-038-11)", "package_ndc": "33342-038-11", "marketing_start_date": "20120911"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 CARTON (33342-038-12)", "package_ndc": "33342-038-12", "marketing_start_date": "20120911"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (33342-038-15)", "package_ndc": "33342-038-15", "marketing_start_date": "20150909"}], "brand_name": "Escitalopram Oxalate", "product_id": "33342-038_53210109-53db-4d08-8ea4-be60e5597caf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "33342-038", "generic_name": "Escitalopram Oxalate", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/21"}], "application_number": "ANDA202210", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}