methylphenidate hydrochloride
NDC 0591-3869, methylphenidate hydrochloride, capsule, extended release, from Actavis Pharma, Inc..
- Product NDC
- 0591-3869
- Status
- Listed
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208861
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3869 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYLPHENIDATE HYDROCHLORIDE20 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0591-3869-19 | 00591386919 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0591-3869-19) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/ecbb4a30-21ac-42e1-b4e9-6c35344ffc45
Use it
Look up 0591-3869 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3869 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0591-3869. 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.