Package 68071-4985-3

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 68071-4985-3
Digits Only 6807149853
Product NDC 68071-4985
Product ID 68071-4985_1b2eab54-08e3-1354-e063-6394a90a2faa
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-4985-3)

Marketing

Marketing Status
Marketed Since 2019-07-25
Brand escitalopram
Generic escitalopram
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": "1b2eab54-08e3-1354-e063-6394a90a2faa", "openfda": {"upc": ["0368071498530"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["8e88bc86-d5e2-50ca-e053-2995a90a0f0e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4985-3)", "package_ndc": "68071-4985-3", "marketing_start_date": "20190725"}], "brand_name": "Escitalopram", "product_id": "68071-4985_1b2eab54-08e3-1354-e063-6394a90a2faa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-4985", "generic_name": "Escitalopram", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA202389", "marketing_category": "ANDA", "marketing_start_date": "20130321", "listing_expiration_date": "20261231"}