Package 70518-2472-1

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 70518-2472-1
Digits Only 7051824721
Product NDC 70518-2472
Product ID 70518-2472_4a2a3df8-60e1-6fcd-e063-6294a90a519e
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2472-1)

Marketing

Marketing Status
Marketed Since 2020-04-22
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": "4a2a3df8-60e1-6fcd-e063-6294a90a519e", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["b6fbd554-9da7-40fd-87a5-2c4af2aa3e6c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2472-1)", "package_ndc": "70518-2472-1", "marketing_start_date": "20200422"}], "brand_name": "Escitalopram", "product_id": "70518-2472_4a2a3df8-60e1-6fcd-e063-6294a90a519e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2472", "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": "20191206", "listing_expiration_date": "20271231"}