Package 55154-6893-0

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 55154-6893-0
Digits Only 5515468930
Product NDC 55154-6893
Description

10 BLISTER PACK in 1 BAG (55154-6893-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-10-15
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb304eb1-adb2-49a1-bcc6-a8575350f2fb", "openfda": {"upc": ["0055154689304"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351250"], "spl_set_id": ["cb3f9af4-5bb4-48a8-b972-ff92cff1ea01"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-6893-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-6893-0", "marketing_start_date": "20141015"}], "brand_name": "escitalopram", "product_id": "55154-6893_eb304eb1-adb2-49a1-bcc6-a8575350f2fb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55154-6893", "generic_name": "escitalopram", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20141015", "listing_expiration_date": "20261231"}