Package 70748-390-01

Brand: prucalopride

Generic: prucalopride
NDC Package

Package Facts

Identity

Package NDC 70748-390-01
Digits Only 7074839001
Product NDC 70748-390
Product ID 70748-390_b9640796-d193-4aff-b1d3-9399b0607d5c
Description

30 TABLET, FILM COATED in 1 BOTTLE (70748-390-01)

Marketing

Marketing Status
Marketed Since 2025-06-25
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": "b9640796-d193-4aff-b1d3-9399b0607d5c", "openfda": {"unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["124e8e82-972d-4800-9d68-14db416959b5"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70748-390-01)", "package_ndc": "70748-390-01", "marketing_start_date": "20250625"}], "brand_name": "Prucalopride", "product_id": "70748-390_b9640796-d193-4aff-b1d3-9399b0607d5c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "70748-390", "generic_name": "Prucalopride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prucalopride", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "2 mg/1"}], "application_number": "ANDA218847", "marketing_category": "ANDA", "marketing_start_date": "20250625", "listing_expiration_date": "20271231"}