United States· US:87143-300_ba4b6a09-9cc9-4617-8c81-b09ecca5fb9e

Pellix

A medicinal product containing calcipotriene, registered in United States by Perfero Pharma, Inc..

US 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…normalisedPellixATC—REGISTER NO.US:87143-300_ba4b6a09…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CALCIPOTRIENE
Manufacturer
Perfero Pharma, Inc.
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    8714330060
    1 BOTTLE, PLASTIC in 1 CARTON (87143-300-60) / 60 mL in 1 BOTTLE, PLASTIC
  • ndc11
    87143-300-60

Regulatory notes

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

Same medicine, other countries

Calcipotriene in 12 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All calcipotriene products

Authorised across Europe · EMA

The same active substance is authorised in 14 EEA countries. Names it is sold under:

  • Austria · Psorcutan
  • Germany · Calcipotriol Hexal, Daivonex
  • Denmark · Calcipotriol Sandoz, Daivonex
  • Spain · Daivonex
  • Finland · Calcipotriol Sandoz
  • France · Daivonex
  • United Kingdom (Northern Ireland) · Calcipotriol Sandoz, Dovonex
  • Greece · Psoraffect
  • Ireland · Dovonex
  • Italy · Calcipotriolo Sandoz, Daivonex
  • Malta · Dovonex
  • Netherlands · Calcipotriol Nevik, Calcipotriol Sandoz
  • Norway · Calcipotriol Sandoz
  • Slovenia · Sorel

Source: European Medicines Agency, Article 57 product data.

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/7cd881ee-4f0e-4cc2-8158-e3a55811bd07
GET /v1/drugs/7cd881ee-4f0e-4cc2-8158-e3a55811bd07?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": "TOPICAL",
  "source": "ndc",
  "strength": ".05",
  "substance": "CALCIPOTRIENE",
  "productndc": "87143-300",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "ANDA078468",
  "marketing_category": "ANDA"
}

See everything about calcipotriene.

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.