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Dissolution Methods Database

Metadata Updated: April 6, 2021

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

Access & Use Information

Public: This dataset is intended for public access and use. License: See this page for license information.

Downloads & Resources

References

http://www.accessdata.fda.gov/scripts/cder/dissolution/index.cfm

Dates

Metadata Created Date November 10, 2020
Metadata Updated Date April 6, 2021
Data Update Frequency R/P3M

Metadata Source

Harvested from Healthdata.gov

Additional Metadata

Resource Type Dataset
Metadata Created Date November 10, 2020
Metadata Updated Date April 6, 2021
Publisher U.S. Food and Drug Administration
Unique Identifier Unknown
Maintainer
Identifier 3f2b8dee-6c80-4230-8f8a-3f7c83920d42
Data First Published 2021-02-25
Data Last Modified 2021-03-12
Public Access Level public
Data Update Frequency R/P3M
Bureau Code 009:10
Metadata Context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
Metadata Catalog ID https://healthdata.gov/data.json
Schema Version https://project-open-data.cio.gov/v1.1/schema
Catalog Describedby https://project-open-data.cio.gov/v1.1/schema/catalog.json
Harvest Object Id 915162fe-5a16-48bc-ae8f-0883f1970ada
Harvest Source Id 651e43b2-321c-4e4c-b86a-835cfc342cb0
Harvest Source Title Healthdata.gov
Homepage URL http://www.fda.gov/Drugs/InformationOnDrugs/ucm135742.htm
License http://opendefinition.org/licenses/odc-odbl/
Program Code 009:002
Related Documents http://www.accessdata.fda.gov/scripts/cder/dissolution/index.cfm
Source Datajson Identifier True
Source Hash b10e7e689abb782bc8908f4982743781695ebe23
Source Schema Version 1.1

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