Package 70518-4567-0

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 70518-4567-0
Digits Only 7051845670
Product NDC 70518-4567
Product ID 70518-4567_4a13e11b-5f03-a0c1-e063-6294a90aa2f6
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4567-0)

Marketing

Marketing Status
Marketed Since 2026-02-04
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": "4a13e11b-5f03-a0c1-e063-6294a90aa2f6", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["0ef807d2-5d66-40c2-be3e-ff6176a35295"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4567-0)", "package_ndc": "70518-4567-0", "marketing_start_date": "20260204"}], "brand_name": "Escitalopram", "product_id": "70518-4567_4a13e11b-5f03-a0c1-e063-6294a90aa2f6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4567", "generic_name": "Escitalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20260204", "listing_expiration_date": "20271231"}