A medicinal product in the final form which is suitable for administering to a patient (after any mixing of multiple components, dissolution etc. has been performed).

An identifier for the administrable product.

The status of this administrable product. Enables tracking the life-cycle of the content.

Allows filtering of administrable products that are appropriate for use versus not.

The medicinal product that this is a prepared administrable form of. This element is not a reference to the item(s) that make up this administrable form (for which see AdministrableProductDefinition.producedFrom). It is medicinal product as a whole, which may have several components (as well as packaging, devices etc.), that are given to the patient in this final administrable form. A single medicinal product may have several different administrable products (e.g. a tablet and a cream), and these could have different administrable forms (e.g. tablet as oral solid, or tablet crushed).

The dose form of the final product after necessary reconstitution or processing. Contrasts to the manufactured dose form (see ManufacturedItemDefinition). If the manufactured form was 'powder for solution for injection', the administrable dose form could be 'solution for injection' (once mixed with another item having manufactured form 'solvent for solution for injection').

The presentation type in which this item is given to a patient. e.g. for a spray - 'puff' (as in 'contains 100 mcg per puff'), or for a liquid - 'vial' (as in 'contains 5 ml per vial').

The constituent manufactured item(s) that this administrable product is produced from. Either a single item, or several that are mixed before administration (e.g. a power item and a solvent item, to make a consumable solution). Note the items this is produced from are not raw ingredients (see AdministrableProductDefinition.ingredient), but manufactured medication items (ManufacturedItemDefinitions), which may be combined or prepared and transformed for patient use. The constituent items that this administrable form is produced from are all part of the product (for which see AdministrableProductDefinition.formOf).

The ingredients of this administrable medicinal product. This is only needed if the ingredients are not specified either using ManufacturedItemDefiniton (via AdministrableProductDefinition.producedFrom) to state which component items are used to make this, or using by incoming references from the Ingredient resource, to state in detail which substances exist within this. This element allows a basic coded ingredient to be used.

A device that is integral to the medicinal product, in effect being considered as an "ingredient" of the medicinal product. This is not intended for devices that are just co-packaged.

Characteristics e.g. a products onset of action.

A code expressing the type of characteristic.

A value for the characteristic.

The status of characteristic e.g. assigned or pending.

The path by which the product is taken into or makes contact with the body. In some regions this is referred to as the licenced or approved route.

Coded expression for the route.

The first dose (dose quantity) administered can be specified for the product, using a numerical value and its unit of measurement.

The maximum single dose that can be administered, can be specified using a numerical value and its unit of measurement.

The maximum dose per day (maximum dose quantity to be administered in any one 24-h period) that can be administered.

The maximum dose per treatment period that can be administered.

The maximum treatment period during which an Investigational Medicinal Product can be administered.

A species for which this route applies.

Coded expression for the species.

A species specific time during which consumption of animal product is not appropriate.

Coded expression for the type of tissue for which the withdrawal period applues, e.g. meat, milk.

A value for the time.

Extra information about the withdrawal period.