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    Drug Ingredients and Development Process

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    Deployed on AWS
    This data package provides information on inactive ingredients present in FDA-approved drug products as well as dissolution methods presently recommended by the Food and Drug Administration (FDA) for drug products that do not have dissolution test methods in the United States Pharmacopeia (USP). It also includes a fraction of the potentially hazardous products with hidden ingredients marketed to consumers on the internet and in retail establishments.

    Overview

    Overview

    This data package gives access to FDA inactive ingredients data. For new drug development purposes, once an inactive ingredient has appeared in an approved drug product for a particular route of administration, the inactive ingredient is not considered new and may require a less extensive review the next time it is included in a new drug product. The data package also includes the FDA Drug Dissolution Methods data that FDA is providing to aid industry personnel in developing generic drug products. The data package also enlists potentially hazardous products with hidden ingredients marketed to consumers on the internet and in retail establishments.


    License Information

    The use of John Snow Labs datasets is free for personal and research purposes. For commercial use please subscribe to the Data Library  on AWS. The subscription will allow you to use all John Snow Labs datasets and data packages for commercial purposes.


    Metadata

    DescriptionValue
    Data Package ComplexitySimple
    Available EnrichmentsN/A
    KeywordsInactive Ingredients, UNII, FDA Registration, FDA Regulations, Inactive Ingredients, FDA Approval Calendar, FDA Inactive Ingredients, Unique Ingredient Identifier, Dissolution Methods, Dissolution Test Method
    Other TitlesFDA Drug Ingredients and Development Process, US Drug Ingredients and Development Process

    Included Datasets

    1. Drugs Inactive Ingredients Database

    The Inactive Ingredient Database provides information on inactive ingredients present in Food and Drug Administration (FDA) approved drug products. This information can be used by industry as an aid in developing drug products.

    1. FDA Drug Dissolution Methods

    For a drug product that does not have a dissolution test method in the United States Pharmacopeia (USP), the Food and Drug Administration (FDA) Dissolution Methods Database provides information on dissolution methods presently recommended by the Division of Bioequivalence, Office of Generic Drugs.

    1. Tainted Products Marketed as Dietary Supplements

    The tainted products marketed as dietary supplements dataset includes a small fraction of the potentially hazardous products with hidden ingredients marketed to consumers on the internet and in retail establishments.


    Data Engineering Overview

    We deliver high-quality data

    • Each dataset goes through 3 levels of quality review
      • 2 Manual reviews are done by domain experts
      • Then, an automated set of 60+ validations enforces every datum matches metadata & defined constraints
    • Data is normalized into one unified type system
      • All dates, unites, codes, currencies look the same
      • All null values are normalized to the same value
      • All dataset and field names are SQL and Hive compliant
    • Data and Metadata
      • Data is available in both CSV and Apache Parquet format, optimized for high read performance on distributed Hadoop, Spark & MPP clusters
      • Metadata is provided in the open Frictionless Data standard, and its every field is normalized & validated
    • Data Updates
      • Data updates support replace-on-update: outdated foreign keys are deprecated, not deleted

    Our data is curated and enriched by domain experts

    Each dataset is manually curated by our team of doctors, pharmacists, public health & medical billing experts:

    • Field names, descriptions, and normalized values are chosen by people who actually understand their meaning
    • Healthcare & life science experts add categories, search keywords, descriptions and more to each dataset
    • Both manual and automated data enrichment supported for clinical codes, providers, drugs, and geo-locations
    • The data is always kept up to date – even when the source requires manual effort to get updates
    • Support for data subscribers is provided directly by the domain experts who curated the data sets
    • Every data source’s license is manually verified to allow for royalty-free commercial use and redistribution.

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    About Us

    John Snow Labs , an AI and NLP for healthcare company, provides state-of-the-art software, models, and data to help healthcare and life science organizations build, deploy, and operate AI projects.

    Details

    Delivery method

    Deployed on AWS
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    Pricing

    Drug Ingredients and Development Process

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    This product is available free of charge. Free subscriptions have no end date and may be canceled any time.
    Additional AWS infrastructure costs may apply. Use the AWS Pricing Calculator  to estimate your infrastructure costs.

    Vendor refund policy

    No refunds offered. For any questions email us at info@johnsnowlabs.com 

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    Legal

    Vendor terms and conditions

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    Usage information

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    Delivery details

    AWS Data Exchange (ADX)

    AWS Data Exchange is a service that helps AWS easily share and manage data entitlements from other organizations at scale.

    Additional details

    Data sets (3)

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    You will receive access to the following data sets.

    Data set name
    Type
    Historical revisions
    Future revisions
    Sensitive information
    Data dictionaries
    Data samples
    Drugs Inactive Ingredients Database
    All historical revisions
    All future revisions
    Not included
    FDA Drug Dissolution Methods
    All historical revisions
    All future revisions
    Not included
    Tainted Products Marketed as Dietary Supplements
    All historical revisions
    All future revisions
    Not included

    Resources

    Vendor resources

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