Package 31722-391-30

Brand: prucalopride

Generic: prucalopride
NDC Package

Package Facts

Identity

Package NDC 31722-391-30
Digits Only 3172239130
Product NDC 31722-391
Description

30 TABLET, FILM COATED in 1 BOTTLE (31722-391-30)

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": "3838bb90-90bd-c65b-e063-6294a90a3e29", "openfda": {"upc": ["0331722392303", "0331722391306"], "unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["4a519883-9231-4ed3-966a-8d9fdbf4a3ac"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-391-30)", "package_ndc": "31722-391-30", "marketing_start_date": "20250624"}], "brand_name": "PRUCALOPRIDE", "product_id": "31722-391_3838bb90-90bd-c65b-e063-6294a90a3e29", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "31722-391", "generic_name": "PRUCALOPRIDE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRUCALOPRIDE", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "1 mg/1"}], "application_number": "ANDA219160", "marketing_category": "ANDA", "marketing_start_date": "20250624", "listing_expiration_date": "20261231"}