Detailed definition of a medicinal product, typically for uses other than direct patient care (e.g. regulatory use, drug catalogs, to support prescribing, adverse events management etc.).

MedicinalProductDefinition
identifier
Business identifier for this product. Could be an MPID
type
Regulatory type, e.g. Investigational or Authorized
domain
If this medicine applies to human or veterinary uses
version
A business identifier relating to a specific version of the product
status
The status within the lifecycle of this product record
statusDate
The date at which the given status became applicable
description
General description of this product
combinedPharmaceuticalDoseForm
The dose form for a single part product, or combined form of a multiple part product
route
The path by which the product is taken into or makes contact with the body
indication
Description of indication(s) for this product, used when structured indications are not required
legalStatusOfSupply
The legal status of supply of the medicinal product as classified by the regulator
additionalMonitoringIndicator
Whether the Medicinal Product is subject to additional monitoring for regulatory reasons
specialMeasures
Whether the Medicinal Product is subject to special measures for regulatory reasons
pediatricUseIndicator
If authorised for use in children
classification
Allows the product to be classified by various systems
marketingStatus
Marketing status of the medicinal product, in contrast to marketing authorization
packagedMedicinalProduct
Package type for the product
comprisedOf
Types of medicinal manufactured items and/or devices that this product consists of, such as tablets, capsule, or syringes
ingredient
The ingredients of this medicinal product - when not detailed in other resources
impurity
Any component of the drug product which is not the chemical entity defined as the drug substance, or an excipient in the drug product
attachedDocument
Additional documentation about the medicinal product
masterFile
A master file for the medicinal product (e.g. Pharmacovigilance System Master File)
contact
A product specific contact, person (in a role), or an organization
type
Allows the contact to be classified, for example QPPV, Pharmacovigilance Enquiry Information
contact
A product specific contact, person (in a role), or an organization
clinicalTrial
Clinical trials or studies that this product is involved in
code
A code that this product is known by, within some formal terminology
name
The product's name, including full name and possibly coded parts
productName
The full product name
type
Type of product name, such as rINN, BAN, Proprietary, Non-Proprietary
part
Coding words or phrases of the name
part
A fragment of a product name
type
Identifying type for this part of the name (e.g. strength part)
usage
Country and jurisdiction where the name applies
country
Country code for where this name applies
jurisdiction
Jurisdiction code for where this name applies
crossReference
Reference to another product, e.g. for linking authorised to investigational product
product
Reference to another product, e.g. for linking authorised to investigational product
type
The type of relationship, for instance branded to generic or virtual to actual product
operation
A manufacturing or administrative process for the medicinal product
type
The type of manufacturing operation e.g. manufacturing itself, re-packaging
effectiveDate
Date range of applicability
organization
The organization responsible for the particular process, e.g. the manufacturer or importer
confidentialityIndicator
Specifies whether this process is considered proprietary or confidential
characteristic
Key product features such as "sugar free", "modified release"
type
A code expressing the type of characteristic
value[x]
A value for the characteristic