Package 70518-1103-0

Brand: Escitalopram

Generic: Escitalopram Oxalate
NDC Package

Package Facts

Identity

Package NDC 70518-1103-0
Digits Only 7051811030
Product NDC 70518-1103
Product ID 70518-1103_4859d5a0-7c37-17bb-e063-6394a90acce0
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1103-0)

Marketing

Marketing Status
Marketed Since 2018-04-09
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": "4859d5a0-7c37-17bb-e063-6394a90acce0", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["32780ff1-0f59-467f-b27f-e541e4c0c7d3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1103-0)", "package_ndc": "70518-1103-0", "marketing_start_date": "20180409"}], "brand_name": "Escitalopram", "product_id": "70518-1103_4859d5a0-7c37-17bb-e063-6394a90acce0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1103", "generic_name": "Escitalopram Oxalate", "labeler_name": "REMEDYREPACK INC.", "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": "20180409", "listing_expiration_date": "20271231"}