Package 60760-894-30

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 60760-894-30
Digits Only 6076089430
Product NDC 60760-894
Product ID 60760-894_3623240f-a96f-d97b-e063-6394a90a9ab6
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-894-30)

Marketing

Marketing Status
Marketed Since 2025-05-19
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": "3623240f-a96f-d97b-e063-6394a90a9ab6", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["362327ce-2dde-f657-e063-6394a90a0b63"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-894-30)", "package_ndc": "60760-894-30", "marketing_start_date": "20250519"}], "brand_name": "escitalopram", "product_id": "60760-894_3623240f-a96f-d97b-e063-6394a90a9ab6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-894", "generic_name": "escitalopram", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}