Products_Drug | R Documentation |
A list of commercially available products in Canada and the United States that contain the drug.
Products_Drug
a tibble with 19 variables:
The proprietary name(s) provided by the manufacturer for any commercially available products containing this drug.
The corporation responsible for labelling this product.
The National Drug Code (NDC) identifier of the drug.
The National Drug Code (NDC) product code from the FDA National Drug Code directory.
Drug Product Database (DPD) identification number (a.k.a. DIN) from the Canadian Drug Product Database. Only present for drugs that are marketed in Canada.
EMA product code from the European Medicines Agency Database. Only present for products that are authorised by central procedure for marketing in the European Union.
EMA marketing authorisation number from the European Medicines Agency Database. Only present for products that are authorised by central procedure for marketing in the European Union.
The starting date for market approval.
The ending date for market approval.
The pharmaceutical formulation by which the drug is introduced into the body.
The amount of active drug ingredient provided in the dosage.
The path by which the drug or product is taken into the body.
The New Drug Application [NDA] number assigned to this drug by the FDA.
A list of Over The Counter (OTC) forms of the drug
Whether this product is a generic drug
Indicates whether this drug has been approved by the regulating government.
The country where this commercially available drug has been approved.
Source of this product information. For example, a value of DPD indicates this information was retrieved from the Canadian Drug Product Database.
drugbank id
Each drug may have one or more product.
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