United States· US:60468-007_4031b751-a798-3024-e063-6294a90ac2b4

Sephience

A sepiapterin product containing sepiapterin, registered in United States by allphamed Pharbil Arzneimittel GmbH. The same ATC class is registered in 9 of our 19 countries.

ATC A16AX28US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedSephienceATCA16AX28REGISTER NO.US:60468-007_4031b751…PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Sepiapterin is registered in 9 of 19 countries.

Countries holding a registration under ATC A16AX28 (sepiapterin), each read from that country’s own register.

  • This record: United States, from FDA National Drug Code directory (United States)
  • 5 of them publish a price we can compare per daily dose

Sepiapterin · ATC A16AX28

9 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Franceprice
  • Icelandprice
  • Ireland
  • Japan
  • Netherlands
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
SEPIAPTERIN
Manufacturer
allphamed Pharbil Arzneimittel GmbH
Country
United States (US)
ATC code
A16AX28
ATC class
Sepiapterin
Defined daily dose
4.25 g, O
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    6046800703
    30 PACKET in 1 CARTON (60468-007-03) / 1 POWDER in 1 PACKET (60468-007-01)
  • ndc11
    60468-007-03

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/d83e4dc9-d729-401b-94e9-4791001f6547
GET /v1/drugs/d83e4dc9-d729-401b-94e9-4791001f6547?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "250",
  "substance": "SEPIAPTERIN",
  "productndc": "60468-007",
  "dosage_form": "POWDER",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "NDA219666",
  "marketing_category": "NDA"
}

See everything about sepiapterin.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.