Methylphenidate Hydrochloride
NDC 13811-709, Methylphenidate hydrochloride, tablet, extended release, from Trigen Laboratories, LLC.
- Product NDC
- 13811-709
- Status
- Listed
- Labeler
- Trigen Laboratories, LLC
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205327
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/13811-709 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYLPHENIDATE HYDROCHLORIDE54 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 13811-709-10 | 13811070910 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-709-10) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/c45dc1de-adfa-4b3c-a7dc-cffbc8eac74fNADAC price for package 13811070910
GET /v1/drugs/nadac/13811070910
Use it
Look up 13811-709 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/13811-709 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 13811-709. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.