capType“The type of container cap. In some cases, it is important for this to be consistent with decapping, piercing or other automated manipulation. Notions such as "child-proof cap" or "resealable bag" may also be indicated here.” - HL7 Version 3 (PackagedProduct.capTypeCode).
codeThis property is used to identify the packaged product (or “sale-able item”), using any coding system except the National Drug Code (NDC), as we have created a separate property for NDC. HL7 and NCPDP both have a single property (which could be multi-valued) to hold any and all such codes in one place, but in the FHIM, we identify the NDC separately due to its importance in federal implementations.“The item code for a packaged product (e.g., complete National Drug Code [NDC] in the U.S.)” - HL7 Version 3 (PackagedProduct.code)."Code to identify the type of product ID contained in CDI03 [Product ID]." - ASAP Standard for PDMP, CDI02: Product ID Qualifier. Possible values include: NDC; UPC; HRI; UPN; DIN."Full product identification as indicated in CDI02 [Product ID Qualifier], including leading zeros without punctuation." - ASAP Standard for PDMP, CDI03: Product ID
codeModifierThis property is used to further identify the packaged product (or “sale-able item”), when the coding system used in the “code” property uses separate code modifiers.
description“A text description of the packaged product. This may include a discussion of the container.” - HL7 Version 3 (PackagedProduct.desc).
labelerPointer to an organization that repackages medicinal products for sale.
medicinalProductPointer to a product produced and marketed as a medicine or drug.
name“A name for the packaged product, usually the same as the name of the product (except where the name contains some reference to the packaging (e.g., "tempo super-pack", "tic-tac easy-box")).” - HL7 Version 3 (PackagedProduct.name).
nationalDrugCode"Each drug product listed under Section 510 of the Federal Food, Drug, and Cosmetic Act is assigned a unique 10-digit, 3-segment number. This number, known as the National Drug Code (NDC), identifies the labeler/vendor, product, and trade package size." - FDA.
packageCapacity"Contains the size of package to be dispensed." - HL7 Version 2.8, RXD-22."Contains the units in which [packageCapacity] is denominated. The advertised number of units in the manufacturer's package, i.e., the package as it comes from the supplier." - HL7 Version 2.8, RXD-23.“Captures the number of product units the package would contain if fully loaded.” - HL7 Version 3 (PackagedProduct.capacityQuantity)."Specific amount of the drug in the packaged product. For example, when specifying a product that has the same strength (For example, Insulin glargine 100 unit per mL solution for injection), this attribute provides additional clarification of the package amount (For example, 3 mL, 10mL, etc)." - HL7 FHIR, Medication.amount
packageType“The package type, such as box or bottle.” - HL7 Version 3 (PackagedProduct.formCode)."The kind of container that this package comes as." - HL7 FHIR, Medication.package.container
productInstancePointer to instances (e.g., particular bottles) of a Packaged Medicinal Product, which will be identified by a serial number or a lot number. For example, if the Packaged Medicinal Product represents all 30-count bottles of Acme Aspirin, this property points to a specific bottle manufactured on Jan. 27th 2016.