Dexmethylphenidate Hydrochloride
NDC 43386-860, Dexmethylphenidate Hydrochloride, tablet, from Lupin Pharmaceuticals,Inc..
- Product NDC
- 43386-860
- Status
- Listed
- Labeler
- Lupin Pharmaceuticals,Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204534
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/43386-860 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DEXMETHYLPHENIDATE HYDROCHLORIDE5 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 43386-860-01 | 43386086001 | 100 TABLET in 1 BOTTLE (43386-860-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/a61932ef-c2b6-4363-a21d-1f0358f317b6
Use it
Look up 43386-860 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43386-860 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43386-860. 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.