Package 51655-149-52

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 51655-149-52
Digits Only 5165514952
Product NDC 51655-149
Product ID 51655-149_48c3f3e4-25a2-6aa7-e063-6394a90a0057
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-52)

Marketing

Marketing Status
Marketed Since 2021-05-07
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": "48c3f3e4-25a2-6aa7-e063-6394a90a0057", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["d9ba6c65-22bd-10c4-e053-2995a90ada2e"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-26)", "package_ndc": "51655-149-26", "marketing_start_date": "20220209"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-52)", "package_ndc": "51655-149-52", "marketing_start_date": "20210507"}], "brand_name": "Escitalopram", "product_id": "51655-149_48c3f3e4-25a2-6aa7-e063-6394a90a0057", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-149", "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": "ANDA202389", "marketing_category": "ANDA", "marketing_start_date": "20210507", "listing_expiration_date": "20271231"}