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    The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products. Spl documents contain both the content of labeling (all text, tables and figures) for a product along with additional machine readable information (including drug listing data elements and clinical data elements). Spl documents can be exchanged across systems without the need for additional transformation steps.

    Drug listing data elements include coded information about the product (including product and generic names, ingredients, ingredient strengths, dosage forms, routes of administration, appearance, dea schedule) and the packaging (package quantity and type). This includes original manufacturers, repackagers, relabelers, and public agencies or private information publishers that submit product information documents. This information is for informational purposes only and is not meant to be a substitute for professional medical advice, diagnosis or treatment.

    Recipients of product label documents are any person or organization, including the public at large, or an agent of the public (such as a regulatory authority). Goodrxs cash prices are based on multiple sources, including published price lists, purchases, claims records, and data provided by pharmacies. All trademarks, brands, logos and copyright images are property of their respective owners and rights holders and are used solely to represent the products of these rights holders.

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    Clinical data elements include coded information about the clinical use of the product (including indications and use, contraindications, drug interactions, warning and precautions and use in special populations). Youll receive an email if the price changes significantly or if theres news about this drug. The prices we show are our best estimate while we believe our data to be generally accurate, we cannot guarantee that the price we display will exactly match the price you receive at the pharmacy. Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location. Implementation guide provides technical conformance criteria for spl  files based on the drug establishment registration and drug listing process at the united states food and drug administration (fda).


    HL7 Version 3 Standard: Structured Product Labeling, Release 4


    HL7 Version 3 Standard: Structured Product Labeling, Release 4 DESCRIPTION. The HL7 Version 3 Structured Product Labeling (SPL) specification is a document markup ...

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    Goodrx is not offering advice, recommending or endorsing any specific prescription drug, pharmacy or other information on the site. This specification includes a detailed description of an information model for structured product labeling documents as well as the xml representation of that model. Youll receive an email if the price changes significantly or if theres news about this drug. The need to create spl documents is typically governed by legal statutes which set points such as the completion of a new drug application (nda), the change of product information or annual reports as requiring submission of an spl document. Spl document is created by an organization that is required by law to submit product information document because it is responsible for the creation or marketing of a product, or any other person or organization compelled by other motives to submit information about products, whether originally created or not.

    Spl documents can be exchanged across systems without the need for additional transformation steps. Hl7 version 3 standard structured product labeling, release 4 may also go by the following names or acronyms facilitates provision of the content of product labeling both electronically and in a human readable format. All trademarks, brands, logos and copyright images are property of their respective owners and rights holders and are used solely to represent the products of these rights holders. Dimenhydrinate (generic dramamine), dosing, proper use and what to know before beginning treatment, imagespage see images of dimenhydrinate (generic dramamine), including the medication and its packaging, latestnewspage news and savings tips created by doctors and pharmacists for dimenhydrinate (generic dramamine), savingspage tips and ways to save for dimenhydrinate (generic dramamine), defaultimage , mobilecanonicallink httpsm. Implementation guide provides technical conformance criteria for spl  files based on the drug establishment registration and drug listing process at the united states food and drug administration (fda). . Improves dissemination of product labeling (both new product labeling and product labeling updates) to users of product labeling. The information model is based on the hl7 reference information model (rim) and uses the hl7 version 3 data types. Access the complete database of hl7 members with the option to search by name, organization, region or affiliate. Drug listing data elements include coded information about the product (including product and generic names, ingredients, ingredient strengths, dosage forms, routes of administration, appearance, dea schedule) and the packaging (package quantity and type).

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