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Lisdexamfetamine dimesylate

Metadata Updated: February 18, 2026

Lisdexamfetamine Dimesylate is a generic prescription medication manufactured by Hikma Pharmaceuticals USA Inc. It's a central nervous system stimulant classified as a DEA Schedule II controlled substance, available in oral capsule form in strengths of 10mg, 20mg, 30mg, 40mg, 50mg, 60mg, and 70mg. This information was generated using AI and is provided for informational and research purposes only.

Access & Use Information

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

Downloads & Resources

Dates

Metadata Created Date February 18, 2026
Metadata Updated Date February 18, 2026
Data Update Frequency R/P1Y

Metadata Source

Harvested from Healthdata.gov

Additional Metadata

Resource Type Dataset
Metadata Created Date February 18, 2026
Metadata Updated Date February 18, 2026
Publisher U.S. Food and Drug Administration
Maintainer
Identifier ANDA202802
Data First Published 2016-09-16
Data Last Modified 2025-03-17
Category FDA
Public Access Level public
Data Update Frequency R/P1Y
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 0b57a21b-c9fb-4702-81bd-661e83eae91a
Harvest Source Id 651e43b2-321c-4e4c-b86a-835cfc342cb0
Harvest Source Title Healthdata.gov
Homepage URL https://www.fda.gov/drugs
License https://open.fda.gov/license
Program Code 009:002
Source Datajson Identifier True
Source Hash 74697a3b20fab8308e92d4ea28e216b0785378547276728b7461728a4c070ab5
Source Schema Version 1.1

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