Package 68071-5248-3

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 68071-5248-3
Digits Only 6807152483
Product NDC 68071-5248
Product ID 68071-5248_1d78c293-2345-7b8b-e063-6394a90ae4e3
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-5248-3)

Marketing

Marketing Status
Marketed Since 2020-04-30
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": "1d78c293-2345-7b8b-e063-6394a90ae4e3", "openfda": {"upc": ["0368071524895"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["a489600b-6ae0-edb7-e053-2a95a90a7d00"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-5248-3)", "package_ndc": "68071-5248-3", "marketing_start_date": "20200430"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-5248-9)", "package_ndc": "68071-5248-9", "marketing_start_date": "20200430"}], "brand_name": "Escitalopram", "product_id": "68071-5248_1d78c293-2345-7b8b-e063-6394a90ae4e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-5248", "generic_name": "Escitalopram", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20120315", "listing_expiration_date": "20261231"}