Package 72578-221-06

Brand: prucalopride

Generic: prucalopride
NDC Package

Package Facts

Identity

Package NDC 72578-221-06
Digits Only 7257822106
Product NDC 72578-221
Product ID 72578-221_6d8aeb40-9dce-4be0-897e-87ad2c5d828e
Description

30 TABLET, FILM COATED in 1 BOTTLE (72578-221-06)

Marketing

Marketing Status
Marketed Since 2026-02-02
Brand prucalopride
Generic prucalopride
Sample Package No

Linked Drug Pages (1)

prucalopride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6d8aeb40-9dce-4be0-897e-87ad2c5d828e", "openfda": {"unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["af559917-802b-486c-9f7b-b770115acac8"], "manufacturer_name": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72578-221-06)", "package_ndc": "72578-221-06", "marketing_start_date": "20260202"}], "brand_name": "prucalopride", "product_id": "72578-221_6d8aeb40-9dce-4be0-897e-87ad2c5d828e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "72578-221", "generic_name": "prucalopride", "labeler_name": "Viona Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prucalopride", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "1 mg/1"}], "application_number": "ANDA218056", "marketing_category": "ANDA", "marketing_start_date": "20260202", "listing_expiration_date": "20271231"}