United States· US:0713-0318_ed81406a-8c10-5c33-e053-2a95a90a941f
Calcipotriene
A medicinal product containing calcipotriene, registered in United States by Cosette Pharmaceuticals, Inc..
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- CALCIPOTRIENE
- Manufacturer
- Cosette Pharmaceuticals, 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
- ndc1107130318531 BOTTLE in 1 CARTON (0713-0318-53) / 60 mL in 1 BOTTLE
- ndc110713-0318-53
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.
- NetherlandsCalcipotriol Sandoz 0,05 mg/ml, oplossing voor cutaan gebruikSandoz B.V.
- United KingdomCalcipotriol 50micrograms/g creamDowelhurst Ltd
- FinlandCalcipotriol SandozSandoz A/S
- GermanyCalcipotriol HexalHexal Ag
- ItalyCALCIPOTRIOLO SANDOZSANDOZ S.P.A.
- BelgiumCalcipotriol/Betamethason Dermapharm 50 µg/g - 0.5 mg/gDermapharm
- IrelandDovonex 50 microgram/g OintmentLeo Laboratories Limited
- SwedenDaivonex 50 mikrogram/g KrämLEO Pharma AB
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/9af7895b-88b9-4026-a6d5-54803fae71a4 GET /v1/drugs/9af7895b-88b9-4026-a6d5-54803fae71a4?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": "0713-0318",
"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.