Package 52427-795-30

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 52427-795-30
Digits Only 5242779530
Product NDC 52427-795
Product ID 52427-795_4caf6d36-950a-522b-5914-079783778c6f
Description

30 CAPSULE in 1 BOTTLE (52427-795-30)

Marketing

Marketing Status
Marketed Since 2025-10-06
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": "4caf6d36-950a-522b-5914-079783778c6f", "openfda": {"upc": ["0352427795305"], "unii": ["5U85DBW7LO"], "rxcui": ["2725159"], "spl_set_id": ["c0401570-a3b0-bef2-7365-c23dc952b8b6"], "manufacturer_name": ["Almatica Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (52427-795-30)", "package_ndc": "52427-795-30", "marketing_start_date": "20251006"}], "brand_name": "escitalopram", "product_id": "52427-795_4caf6d36-950a-522b-5914-079783778c6f", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "52427-795", "generic_name": "escitalopram", "labeler_name": "Almatica Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "15 mg/1"}], "application_number": "NDA219130", "marketing_category": "NDA", "marketing_start_date": "20251006", "listing_expiration_date": "20261231"}