Package 70518-4300-0

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 70518-4300-0
Digits Only 7051843000
Product NDC 70518-4300
Product ID 70518-4300_38f2532b-84e2-7b40-e063-6394a90a4aa0
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4300-0)

Marketing

Marketing Status
Marketed Since 2025-03-03
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": "38f2532b-84e2-7b40-e063-6394a90a4aa0", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["d75e3b97-1ead-4e7b-9ae3-3626aede1efd"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4300-0)", "package_ndc": "70518-4300-0", "marketing_start_date": "20250303"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4300-1)", "package_ndc": "70518-4300-1", "marketing_start_date": "20250701"}], "brand_name": "escitalopram", "product_id": "70518-4300_38f2532b-84e2-7b40-e063-6394a90a4aa0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4300", "generic_name": "escitalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20250303", "listing_expiration_date": "20261231"}