Package 52856-201-03

Brand: sephience

Generic: sepiapterin
NDC Package

Package Facts

Identity

Package NDC 52856-201-03
Digits Only 5285620103
Product NDC 52856-201
Description

30 PACKET in 1 CARTON (52856-201-03) / 1 POWDER in 1 PACKET (52856-201-01)

Marketing

Marketing Status
Marketed Since 2025-07-28
Brand sephience
Generic sepiapterin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1058e322-6878-46c2-917d-3f65c8b36aeb", "openfda": {"upc": ["0352856201033", "0352856301030"], "unii": ["CJQ26KO7HP"], "rxcui": ["2723061", "2723067", "2723069", "2723071"], "spl_set_id": ["32ac719c-49f0-4105-9c46-18c19583a5c2"], "manufacturer_name": ["PTC Therapeutics Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (52856-201-03)  / 1 POWDER in 1 PACKET (52856-201-01)", "package_ndc": "52856-201-03", "marketing_start_date": "20250728"}], "brand_name": "Sephience", "product_id": "52856-201_1058e322-6878-46c2-917d-3f65c8b36aeb", "dosage_form": "POWDER", "product_ndc": "52856-201", "generic_name": "sepiapterin", "labeler_name": "PTC Therapeutics Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sephience", "active_ingredients": [{"name": "SEPIAPTERIN", "strength": "250 mg/1"}], "application_number": "NDA219666", "marketing_category": "NDA", "marketing_start_date": "20250728", "listing_expiration_date": "20261231"}