Package 71610-534-60

Brand: escitalopram oxalate

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71610-534-60
Digits Only 7161053460
Product NDC 71610-534
Product ID 71610-534_2b8bb776-9f66-415a-b869-aded0e844450
Description

90 TABLET, FILM COATED in 1 BOTTLE (71610-534-60)

Marketing

Marketing Status
Marketed Since 2021-03-09
Brand escitalopram oxalate
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Escitalopram oxalate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b8bb776-9f66-415a-b869-aded0e844450", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["900b7a2f-23e7-4c78-bd6e-549bbe09883e"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-534-60)", "package_ndc": "71610-534-60", "marketing_start_date": "20210309"}], "brand_name": "Escitalopram oxalate", "product_id": "71610-534_2b8bb776-9f66-415a-b869-aded0e844450", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71610-534", "generic_name": "escitalopram", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078604", "marketing_category": "ANDA", "marketing_start_date": "20121001", "listing_expiration_date": "20261231"}