Package 70771-1899-3

Brand: prucalopride

Generic: prucalopride
NDC Package

Package Facts

Identity

Package NDC 70771-1899-3
Digits Only 7077118993
Product NDC 70771-1899
Product ID 70771-1899_051f4f7e-88e8-4706-8183-dbd3f9d42d72
Description

30 TABLET, FILM COATED in 1 BOTTLE (70771-1899-3)

Marketing

Marketing Status
Marketed Since 2026-02-02
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": "051f4f7e-88e8-4706-8183-dbd3f9d42d72", "openfda": {"unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["da37395d-0a05-4fdc-ab5c-eb7caed62bf1"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70771-1899-3)", "package_ndc": "70771-1899-3", "marketing_start_date": "20260202"}], "brand_name": "prucalopride", "product_id": "70771-1899_051f4f7e-88e8-4706-8183-dbd3f9d42d72", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "70771-1899", "generic_name": "prucalopride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prucalopride", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "1 mg/1"}], "application_number": "ANDA218056", "marketing_category": "ANDA", "marketing_start_date": "20260202", "listing_expiration_date": "20271231"}