Package 50090-5312-0

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 50090-5312-0
Digits Only 5009053120
Product NDC 50090-5312
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-5312-0)

Marketing

Marketing Status
Marketed Since 2020-10-29
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5d70869d-59cb-4cbe-80a1-0b4106c4eab0", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["9b0b3c54-5bbc-4db9-9c69-00dac1347f24"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5312-0)", "package_ndc": "50090-5312-0", "marketing_start_date": "20201029"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-5312-1)", "package_ndc": "50090-5312-1", "marketing_start_date": "20230713"}], "brand_name": "Escitalopram", "product_id": "50090-5312_5d70869d-59cb-4cbe-80a1-0b4106c4eab0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-5312", "generic_name": "Escitalopram", "labeler_name": "A-S Medication Solutions", "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": "20160201", "listing_expiration_date": "20261231"}