Package 43063-761-30

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 43063-761-30
Digits Only 4306376130
Product NDC 43063-761
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-30)

Marketing

Marketing Status
Marketed Since 2017-05-25
Brand escitalopram oxalate
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "419e34ea-17b4-ec32-e063-6394a90a603d", "openfda": {"upc": ["0343063761304"], "unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["b7670e51-8f44-4f64-b110-3f2f431a4032"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-01)", "package_ndc": "43063-761-01", "marketing_start_date": "20170525"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-30)", "package_ndc": "43063-761-30", "marketing_start_date": "20170525"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-90)", "package_ndc": "43063-761-90", "marketing_start_date": "20170503"}], "brand_name": "escitalopram oxalate", "product_id": "43063-761_419e34ea-17b4-ec32-e063-6394a90a603d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-761", "generic_name": "escitalopram oxalate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}