Package 0781-8158-31

Brand: prucalopride

Generic: prucalopride
NDC Package

Package Facts

Identity

Package NDC 0781-8158-31
Digits Only 0781815831
Product NDC 0781-8158
Product ID 0781-8158_0145490a-4ba4-4b33-8602-4a6e9ca52ff2
Description

30 TABLET, FILM COATED in 1 BOTTLE (0781-8158-31)

Marketing

Marketing Status
Marketed Since 2025-06-13
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": "0145490a-4ba4-4b33-8602-4a6e9ca52ff2", "openfda": {"upc": ["0307818159310"], "unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["6325308c-4b0f-4926-bb85-b63db614533d"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0781-8158-31)", "package_ndc": "0781-8158-31", "marketing_start_date": "20250613"}], "brand_name": "PRUCALOPRIDE", "product_id": "0781-8158_0145490a-4ba4-4b33-8602-4a6e9ca52ff2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "0781-8158", "generic_name": "PRUCALOPRIDE", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRUCALOPRIDE", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "1 mg/1"}], "application_number": "ANDA218963", "marketing_category": "ANDA", "marketing_start_date": "20250613", "listing_expiration_date": "20261231"}