Methylphenidate
NDC 10702-164, Methylphenidate Hydrochloride, solution, from KVK-Tech, Inc..
- Product NDC
- 10702-164
- Status
- Listed
- Labeler
- KVK-Tech, Inc.
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207485
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/10702-164 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYLPHENIDATE HYDROCHLORIDE10 mg/5mL
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 10702-164-50 | 10702016450 | 500 mL in 1 BOTTLE (10702-164-50) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/2cf1b26b-199d-4c7f-ab64-4805a9def2cc
Use it
Look up 10702-164 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/10702-164 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 10702-164. 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.