Package 76282-249-90

Brand: escitalopram oxalate

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 76282-249-90
Digits Only 7628224990
Product NDC 76282-249
Description

90 TABLET, FILM COATED in 1 BOTTLE (76282-249-90)

Marketing

Marketing Status
Marketed Since 2012-10-01
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": "787c121b-d227-4f2f-aa8d-e2dd69790fa6", "openfda": {"upc": ["0376282251103", "0376282250908", "0376282250304", "0376282249100", "0376282251301", "0376282251905", "0376282249902", "0376282249308"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["8a3f4bc9-cd6e-49b1-ab6c-982b70f51fd2"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76282-249-01)", "package_ndc": "76282-249-01", "marketing_start_date": "20121001"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76282-249-05)", "package_ndc": "76282-249-05", "marketing_start_date": "20121001"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (76282-249-10)", "package_ndc": "76282-249-10", "marketing_start_date": "20121001"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76282-249-30)", "package_ndc": "76282-249-30", "marketing_start_date": "20121001"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76282-249-90)", "package_ndc": "76282-249-90", "marketing_start_date": "20121001"}], "brand_name": "Escitalopram oxalate", "product_id": "76282-249_787c121b-d227-4f2f-aa8d-e2dd69790fa6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "76282-249", "generic_name": "escitalopram", "labeler_name": "Exelan Pharmaceuticals 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": "20121001", "listing_expiration_date": "20261231"}