Package 60505-4806-3

Brand: prucalopride

Generic: prucalopride
NDC Package

Package Facts

Identity

Package NDC 60505-4806-3
Digits Only 6050548063
Product NDC 60505-4806
Description

30 TABLET, FILM COATED in 1 BOTTLE (60505-4806-3)

Marketing

Marketing Status
Marketed Since 2025-06-24
Brand prucalopride
Generic prucalopride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06f30acf-a55e-9a8d-e4e2-46d3a7d66639", "openfda": {"upc": ["0360505480630", "0360505480739"], "unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["01dcea95-b391-79da-bbfe-412f39022e9a"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-4806-3)", "package_ndc": "60505-4806-3", "marketing_start_date": "20250624"}], "brand_name": "Prucalopride", "product_id": "60505-4806_06f30acf-a55e-9a8d-e4e2-46d3a7d66639", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "60505-4806", "generic_name": "Prucalopride", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prucalopride", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "1 mg/1"}], "application_number": "ANDA218977", "marketing_category": "ANDA", "marketing_start_date": "20250624", "listing_expiration_date": "20261231"}