Package 83085-005-30

Brand: prucalopride

Generic: prucalopride
NDC Package

Package Facts

Identity

Package NDC 83085-005-30
Digits Only 8308500530
Product NDC 83085-005
Product ID 83085-005_25c68e03-9af5-47da-95ce-ca870a8b531f
Description

30 TABLET, FILM COATED in 1 BOTTLE (83085-005-30)

Marketing

Marketing Status
Marketed Since 2025-06-24
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": "25c68e03-9af5-47da-95ce-ca870a8b531f", "openfda": {"unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["a1488b84-40e4-472a-a34b-68ef37c0260e"], "manufacturer_name": ["SKG Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (83085-005-30)", "package_ndc": "83085-005-30", "marketing_start_date": "20250624"}], "brand_name": "PRUCALOPRIDE", "product_id": "83085-005_25c68e03-9af5-47da-95ce-ca870a8b531f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "83085-005", "generic_name": "PRUCALOPRIDE", "labeler_name": "SKG Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRUCALOPRIDE", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "1 mg/1"}], "application_number": "ANDA218812", "marketing_category": "ANDA", "marketing_start_date": "20250624", "listing_expiration_date": "20261231"}