Package 51655-147-26

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 51655-147-26
Digits Only 5165514726
Product NDC 51655-147
Product ID 51655-147_48c3e3f2-09c4-c403-e063-6294a90aafde
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-147-26)

Marketing

Marketing Status
Marketed Since 2023-01-25
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": "48c3e3f2-09c4-c403-e063-6294a90aafde", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["f6ca64ec-68ff-e1ea-e053-6294a90ae0f8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-147-26)", "package_ndc": "51655-147-26", "marketing_start_date": "20230125"}], "brand_name": "Escitalopram", "product_id": "51655-147_48c3e3f2-09c4-c403-e063-6294a90aafde", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-147", "generic_name": "Escitalopram Oxalate", "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": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20230125", "listing_expiration_date": "20271231"}