Package 71610-425-60

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71610-425-60
Digits Only 7161042560
Product NDC 71610-425
Product ID 71610-425_09b866f0-4435-4d1a-9cc7-c6a5ea487cb0
Description

90 TABLET, FILM COATED in 1 BOTTLE (71610-425-60)

Marketing

Marketing Status
Marketed Since 2020-05-08
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": "09b866f0-4435-4d1a-9cc7-c6a5ea487cb0", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["85b2f57e-53f3-4b93-9128-ad74cc34be4c"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-425-60)", "package_ndc": "71610-425-60", "marketing_start_date": "20200508"}], "brand_name": "Escitalopram", "product_id": "71610-425_09b866f0-4435-4d1a-9cc7-c6a5ea487cb0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71610-425", "generic_name": "Escitalopram", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA202389", "marketing_category": "ANDA", "marketing_start_date": "20130321", "listing_expiration_date": "20261231"}