Package 60760-895-90
Brand: escitalopram
Generic: escitalopramPackage Facts
Identity
Package NDC
60760-895-90
Digits Only
6076089590
Product NDC
60760-895
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-90)
Marketing
Marketing Status
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": "47d4373f-7797-2ab5-e063-6294a90a40c4", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["1b2ec266-be5b-9265-e063-6294a90a10e3"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-30)", "package_ndc": "60760-895-30", "marketing_start_date": "20250513"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-90)", "package_ndc": "60760-895-90", "marketing_start_date": "20240612"}], "brand_name": "escitalopram", "product_id": "60760-895_47d4373f-7797-2ab5-e063-6294a90a40c4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-895", "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": "10 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20271231"}