Package 72205-219-30

Brand: prucalopride

Generic: prucalopride
NDC Package

Package Facts

Identity

Package NDC 72205-219-30
Digits Only 7220521930
Product NDC 72205-219
Description

30 TABLET, FILM COATED in 1 BOTTLE (72205-219-30)

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": "89a7fce6-5d3e-4a71-a86c-06d209951c63", "openfda": {"upc": ["0372205219304", "0372205218307"], "unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["1f195f1d-d509-4f8b-8710-2d0d110b6b5c"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72205-219-30)", "package_ndc": "72205-219-30", "marketing_start_date": "20250624"}], "brand_name": "PRUCALOPRIDE", "product_id": "72205-219_89a7fce6-5d3e-4a71-a86c-06d209951c63", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "72205-219", "generic_name": "PRUCALOPRIDE", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRUCALOPRIDE", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "2 mg/1"}], "application_number": "ANDA218177", "marketing_category": "ANDA", "marketing_start_date": "20250624", "listing_expiration_date": "20271231"}