Package 51655-284-26

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 51655-284-26
Digits Only 5165528426
Product NDC 51655-284
Product ID 51655-284_48e710d5-cd0b-b488-e063-6394a90a8b6b
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-26)

Marketing

Marketing Status
Marketed Since 2020-05-13
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": "48e710d5-cd0b-b488-e063-6394a90a8b6b", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["addccf96-cc60-6045-e053-2a95a90aaac0"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-26)", "package_ndc": "51655-284-26", "marketing_start_date": "20200513"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-284-52)", "package_ndc": "51655-284-52", "marketing_start_date": "20220720"}], "brand_name": "Escitalopram", "product_id": "51655-284_48e710d5-cd0b-b488-e063-6394a90a8b6b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-284", "generic_name": "Escitalopram", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20200513", "listing_expiration_date": "20271231"}