Package 70069-822-01

Brand: prucalopride succinate

Generic: prucalopride succinate
NDC Package

Package Facts

Identity

Package NDC 70069-822-01
Digits Only 7006982201
Product NDC 70069-822
Description

1 BOTTLE in 1 BOTTLE (70069-822-01) / 30 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-06-24
Brand prucalopride succinate
Generic prucalopride succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7b3acc62-d656-47b8-91d2-5b30cd699fbd", "openfda": {"unii": ["4V2G75E1CK"], "rxcui": ["2107345", "2107353"], "spl_set_id": ["1750cd94-b443-49df-9c53-eb5b68f66092"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOTTLE (70069-822-01)  / 30 TABLET in 1 BOTTLE", "package_ndc": "70069-822-01", "marketing_start_date": "20250624"}], "brand_name": "Prucalopride succinate", "product_id": "70069-822_7b3acc62-d656-47b8-91d2-5b30cd699fbd", "dosage_form": "TABLET", "pharm_class": ["Serotonin 4 Receptor Agonists [MoA]", "Serotonin-4 Receptor Agonist [EPC]"], "product_ndc": "70069-822", "generic_name": "Prucalopride succinate", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prucalopride succinate", "active_ingredients": [{"name": "PRUCALOPRIDE SUCCINATE", "strength": "2 mg/1"}], "application_number": "ANDA219078", "marketing_category": "ANDA", "marketing_start_date": "20250624", "listing_expiration_date": "20261231"}