Package 68084-617-01

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 68084-617-01
Digits Only 6808461701
Product NDC 68084-617
Product ID 68084-617_30deba4d-85ab-64e3-e063-6394a90a085e
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-617-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-617-11)

Marketing

Marketing Status
Marketed Since 2012-10-08
Brand escitalopram
Generic escitalopram oxalate
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": "30deba4d-85ab-64e3-e063-6394a90a085e", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351250"], "spl_set_id": ["3019a647-9bcf-48cf-928c-0467f9b921a8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-617-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-617-11)", "package_ndc": "68084-617-01", "marketing_start_date": "20121008"}], "brand_name": "Escitalopram", "product_id": "68084-617_30deba4d-85ab-64e3-e063-6394a90a085e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68084-617", "generic_name": "Escitalopram Oxalate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20121008", "listing_expiration_date": "20261231"}