Package 42708-077-30

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package Sample

Package Facts

Identity

Package NDC 42708-077-30
Digits Only 4270807730
Product NDC 42708-077
Product ID 42708-077_458675e8-3e61-a250-e063-6294a90acf58
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-077-30)

Marketing

Marketing Status
Marketed Since 2018-12-18
Brand escitalopram
Generic escitalopram oxalate
Sample Package Yes

Linked Drug Pages (1)

Escitalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "458675e8-3e61-a250-e063-6294a90acf58", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["85fbcce8-a870-4f04-8a0e-a12e46eed3cf"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-077-30)", "package_ndc": "42708-077-30", "marketing_start_date": "20181218"}], "brand_name": "Escitalopram", "product_id": "42708-077_458675e8-3e61-a250-e063-6294a90acf58", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42708-077", "generic_name": "Escitalopram Oxalate", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}