Dissolution Methods Database

Metadata Updated: July 26, 2023

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

Web PageHTML
ucm135742.htm

Visit page

Landing PageLanding Page

Visit page

References

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

Dates

Metadata Created Date	November 10, 2020
Metadata Updated Date	July 26, 2023
Data Update Frequency	R/P3M

Metadata Source

Data.json Data.json Metadata
Download Metadata

Harvested from Healthdata.gov

Additional Metadata

Resource Type	Dataset
Metadata Created Date	November 10, 2020
Metadata Updated Date	July 26, 2023
Publisher	U.S. Food and Drug Administration
Maintainer	openFDA
Identifier	3f2b8dee-6c80-4230-8f8a-3f7c83920d42
Data First Published	2021-02-25
Data Last Modified	2023-07-25
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	b0c6efab-b868-4cf7-b5f4-46f9cfe75ffb
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	d730f0052dcd2c47f24e3a87a3b2ec0cea99eb26
Source Schema Version	1.1

Didn't find what you're looking for? Suggest a dataset here.