Package 69097-847-12

Brand: escitalopram oxalate

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 69097-847-12
Digits Only 6909784712
Product NDC 69097-847
Description

500 TABLET, FILM COATED in 1 BOTTLE (69097-847-12)

Marketing

Marketing Status
Marketed Since 2016-06-16
Brand escitalopram oxalate
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7e44336f-9692-42ff-af45-f98edd0c803c", "openfda": {"upc": ["0369097847050", "0369097848057"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["31ce0b82-58fe-44f3-8887-c55d8df1b773"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69097-847-02)", "package_ndc": "69097-847-02", "marketing_start_date": "20160616"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (69097-847-05)", "package_ndc": "69097-847-05", "marketing_start_date": "20160616"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69097-847-07)", "package_ndc": "69097-847-07", "marketing_start_date": "20160616"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69097-847-12)", "package_ndc": "69097-847-12", "marketing_start_date": "20160616"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (69097-847-15)", "package_ndc": "69097-847-15", "marketing_start_date": "20160616"}], "brand_name": "Escitalopram Oxalate", "product_id": "69097-847_7e44336f-9692-42ff-af45-f98edd0c803c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "69097-847", "generic_name": "Escitalopram", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078604", "marketing_category": "ANDA", "marketing_start_date": "20160616", "listing_expiration_date": "20261231"}