Package 68071-3069-8

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 68071-3069-8
Digits Only 6807130698
Product NDC 68071-3069
Product ID 68071-3069_1d8e7443-eb23-ccda-e063-6394a90ae343
Description

28 TABLET, FILM COATED in 1 BOTTLE (68071-3069-8)

Marketing

Marketing Status
Marketed Since 2017-03-10
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": "1d8e7443-eb23-ccda-e063-6394a90ae343", "openfda": {"upc": ["0368071306934"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["4a645652-ae1f-3811-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3069-3)", "package_ndc": "68071-3069-3", "marketing_start_date": "20170310"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68071-3069-8)", "package_ndc": "68071-3069-8", "marketing_start_date": "20170310"}], "brand_name": "Escitalopram", "product_id": "68071-3069_1d8e7443-eb23-ccda-e063-6394a90ae343", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-3069", "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"}