United States· US:84015-930_73db4875-9ff1-4eaf-bc83-0e494aada598
PALSONIFY
A paltusotine product containing paltusotine hydrochloride, registered in United States by Crinetics Pharmaceuticals, Inc.. The same ATC class is registered in 9 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Paltusotine is registered in 9 of 19 countries.
Countries holding a registration under ATC H01CB06 (paltusotine), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 6 of them publish a price we can compare per daily dose
Paltusotine · ATC H01CB06
9 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- PALTUSOTINE HYDROCHLORIDE
- Manufacturer
- Crinetics Pharmaceuticals, Inc.
- Country
- United States (US)
- ATC code
- H01CB06
- ATC class
- Paltusotine
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc11840159306060 TABLET, FILM COATED in 1 BOTTLE (84015-930-60)
- ndc1184015-930-60
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Paltusotine in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumPalsonify 30 mgCrinetics Pharmaceuticals Europe
- CzechiaPALSONIFYCrinetics Pharmaceuticals Europe GmbH, Amsterdam
- FinlandPalsonifyCrinetics Pharmaceuticals Europe GmbH
- IrelandPalsonify 30 mg film-coated tabletsVoisin Consulting Life Sciences
- IcelandPalsonifyCrinetics Pharmaceuticals Europe GmbH
- NetherlandsPalsonify 30 mg filmomhulde tablettenCrinetics Pharmaceuticals Europe GmbH
- PolandPalsonify
- SwedenPalsonify 30 mg Filmdragerad tablettCrinetics Pharmaceuticals Europe GmbH
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Iceland · Palsonify
- Norway · Palsonify
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/8d78cbb5-3b1c-4cc1-afd4-04855f500652 GET /v1/drugs/8d78cbb5-3b1c-4cc1-afd4-04855f500652?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": "30",
"substance": "PALTUSOTINE HYDROCHLORIDE",
"productndc": "84015-930",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"strength_unit": "mg/1",
"application_number": "NDA219070",
"marketing_category": "NDA"
}See everything about paltusotine.
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.