Package 68788-8569-6

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 68788-8569-6
Digits Only 6878885696
Product NDC 68788-8569
Description

60 TABLET, FILM COATED in 1 BOTTLE (68788-8569-6)

Marketing

Marketing Status
Marketed Since 2025-04-08
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": "3cb153dc-e977-4848-868a-bce458631a2a", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["d16a7510-c787-4c9b-818b-1ffbcc62b3c3"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-8569-1)", "package_ndc": "68788-8569-1", "marketing_start_date": "20250408"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8569-3)", "package_ndc": "68788-8569-3", "marketing_start_date": "20240123"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8569-6)", "package_ndc": "68788-8569-6", "marketing_start_date": "20250408"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8569-9)", "package_ndc": "68788-8569-9", "marketing_start_date": "20250408"}], "brand_name": "escitalopram", "product_id": "68788-8569_3cb153dc-e977-4848-868a-bce458631a2a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68788-8569", "generic_name": "escitalopram", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20240123", "listing_expiration_date": "20261231"}