Methylphenidate Hydrochloride
NDC 72865-133, Methylphenidate Hydrochloride, tablet, extended release, from XLCare Pharmaceuticals, Inc..
- Product NDC
- 72865-133
- Status
- Listed
- Labeler
- XLCare Pharmaceuticals, Inc.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211009
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/72865-133 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYLPHENIDATE HYDROCHLORIDE18 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72865-133-01 | 72865013301 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-133-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/b07150db-fd99-4400-bb83-b3a7544a917a
Use it
Look up 72865-133 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72865-133 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72865-133. 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.