United States· US:0074-9036_ed8862d9-4037-4a30-9be6-42f2613c34cd

Zemplar

A medicinal product containing paricalcitol, registered in United States by AbbVie Inc..

US label

Checked against FDA National Drug Code directory (United States) on June 3, 2026

Informational only — not a medical device.

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The record

At a glance

FDA National Drug Code directory (United States)

Active substance: Paricalcitol
Manufacturer: AbbVie Inc.
Country: United States (US)
ATC code: —
Reimbursed: Not published by this register
Source register: FDA National Drug Code directory (United States)
Last checked: June 3, 2026

Packs & prices · 1

ndc11
0074903630
30 CAPSULE, LIQUID FILLED in 1 BOTTLE (0074-9036-30)

Regulatory notes

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

Same medicine, other countries

Paricalcitol in 11 other countries

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

All paricalcitol products

Authorised across Europe · EMA

The same active substance is authorised in 23 EEA countries. Names it is sold under:

Austria · Paricalcitol Accord, Zemplar
Bulgaria · Тевапаривит
Cyprus · Rextol
Czechia · Paricalcitol Accord, Paricalcitol Agmed
Germany · Paricalcitol Accord, Paricalcitol Hexal
Denmark · Paricalcitol Pharmathen
Spain · Paricalcitol Accord, Paricalcitol Accordpharma
Finland · Paricalcitol Accord, Paricalcitol Alternova
United Kingdom (Northern Ireland) · Zemplar
Greece · Aricitol, Panozin
Croatia · Parkol, Zemplar
Hungary · Paricalcitol Fresenius, Paricalcitol Onkogen
Ireland · Paricalcitol Pinewood Laboratories, Zemplar
Italy · Paracalcitolo Mylan, Paracalcitolo Sandoz
Luxembourg · Porontazin
Netherlands · Paricalcitol Accord, Paricalcitol Heaton
Norway · Paricalcitol Alternova
Poland · Paricalcitol Fresenius
Portugal · Paricalcitol Accord, Paricalcitol Altan
Romania · Paricalcitol, Rextol
Sweden · Paricalcitol Accord, Paricalcitol Alternova
Slovenia · Zemplar
Slovakia · Paricalcitol Heaton, Zemplar

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/00aebcdf-d50b-40f1-a58b-3ed3d607037b
GET /v1/drugs/00aebcdf-d50b-40f1-a58b-3ed3d607037b?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",
  "productid": "0074-9036_ed8862d9-4037-4a30-9be6-42f2613c34cd",
  "productndc": "0074-9036",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PARICALCITOL",
  "proprietary_name": "Zemplar",
  "active_ingred_unit": "ug/1",
  "application_number": "NDA021606",
  "marketing_category": "NDA",
  "nonproprietary_name": "Paricalcitol",
  "start_marketing_date": "20180420",
  "active_numerator_strength": "1"
}

API reference MCP server Plans

See everything about paricalcitol.

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.

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