Package 51655-277-52

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 51655-277-52
Digits Only 5165527752
Product NDC 51655-277
Product ID 51655-277_48e6f0e2-cba0-fa06-e063-6294a90a296f
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-52)

Marketing

Marketing Status
Marketed Since 2022-09-08
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": "48e6f0e2-cba0-fa06-e063-6294a90a296f", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["f2b7b0a6-481b-1f6f-e053-2a95a90a2d04"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-26)", "package_ndc": "51655-277-26", "marketing_start_date": "20221005"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-52)", "package_ndc": "51655-277-52", "marketing_start_date": "20220908"}], "brand_name": "Escitalopram", "product_id": "51655-277_48e6f0e2-cba0-fa06-e063-6294a90a296f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-277", "generic_name": "Escitalopram", "labeler_name": "Northwind Health Company, LLC", "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": "20220908", "listing_expiration_date": "20271231"}