Dexmethylphenidate hydrochloride
Dexmethylphenidate Hydrochloride Extended-Release is a prescription stimulant medication used to treat attention deficit hyperactivity disorder (ADHD). It comes as extended-release capsules in strengths from 5mg to 40mg, taken orally. Manufactured by Lannett Company, Inc., it's a generic version and a Schedule II controlled substance. This information was generated using AI and is provided for informational and research purposes only.
Complete Metadata
| @type | dcat:Dataset |
|---|---|
| accessLevel | public |
| accrualPeriodicity | R/P1Y |
| bureauCode |
[
"009:10"
]
|
| contactPoint |
{
"fn": "Division of Drug Information",
"@type": "vcard:Contact",
"hasEmail": "mailto:druginfo@fda.hhs.gov"
}
|
| description | Dexmethylphenidate Hydrochloride Extended-Release is a prescription stimulant medication used to treat attention deficit hyperactivity disorder (ADHD). It comes as extended-release capsules in strengths from 5mg to 40mg, taken orally. Manufactured by Lannett Company, Inc., it's a generic version and a Schedule II controlled substance. This information was generated using AI and is provided for informational and research purposes only. |
| distribution |
[
{
"@type": "dcat:Distribution",
"title": "Dexmethylphenidate hydrochloride",
"mediaType": "text/html",
"description": "
Access the FDA dataset for Dexmethylphenidate hydrochloride — ANDA 202842 submitted by Mylan Institutional LLC
",
"downloadURL": "https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=202842"
}
]
|
| identifier | ANDA202842 |
| issued | 2016-09-16 |
| keyword |
[
"drug",
"drug-information",
"health-care",
"pharmaceuticals",
"prescription-drugs"
]
|
| landingPage | https://www.fda.gov/drugs |
| license | https://open.fda.gov/license |
| modified | 2025-03-17 |
| programCode |
[
"009:002"
]
|
| publisher |
{
"name": "U.S. Food and Drug Administration",
"@type": "org:Organization"
}
|
| theme |
[
"FDA"
]
|
| title | Dexmethylphenidate hydrochloride |
