Package 50090-6190-1

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 50090-6190-1
Digits Only 5009061901
Product NDC 50090-6190
Product ID 50090-6190_639f9151-0f94-4585-9132-7ad5efe5a2b0
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6190-1)

Marketing

Marketing Status
Marketed Since 2022-10-28
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": "639f9151-0f94-4585-9132-7ad5efe5a2b0", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["a0344290-6e12-46c4-a11c-5347a770adbe"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6190-0)", "package_ndc": "50090-6190-0", "marketing_start_date": "20221028"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6190-1)", "package_ndc": "50090-6190-1", "marketing_start_date": "20221028"}], "brand_name": "Escitalopram", "product_id": "50090-6190_639f9151-0f94-4585-9132-7ad5efe5a2b0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6190", "generic_name": "Escitalopram", "labeler_name": "A-S Medication Solutions", "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": "20160201", "listing_expiration_date": "20271231"}