Package 51655-116-26

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 51655-116-26
Digits Only 5165511626
Product NDC 51655-116
Product ID 51655-116_48c3d134-d4dc-a5fc-e063-6294a90acd5a
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-26)

Marketing

Marketing Status
Marketed Since 2022-12-01
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": "48c3d134-d4dc-a5fc-e063-6294a90acd5a", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["f2b3b385-658d-5918-e053-2a95a90afcba"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-26)", "package_ndc": "51655-116-26", "marketing_start_date": "20221201"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-116-52)", "package_ndc": "51655-116-52", "marketing_start_date": "20220711"}], "brand_name": "Escitalopram", "product_id": "51655-116_48c3d134-d4dc-a5fc-e063-6294a90acd5a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-116", "generic_name": "Escitalopram", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20220711", "listing_expiration_date": "20271231"}