METHYLPHENIDATE HYDROCHLORIDE EXTENDED RELEASE
NDC 10702-075, methylphenidate hydrochloride extended release, tablet, from KVK-Tech, Inc..
- Product NDC
- 10702-075
- Status
- Listed
- Labeler
- KVK-Tech, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207488
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/10702-075 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYLPHENIDATE HYDROCHLORIDE10 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 10702-075-01 | 10702007501 | 100 TABLET in 1 BOTTLE (10702-075-01) |
| 10702-075-06 | 10702007506 | 60 TABLET in 1 BOTTLE (10702-075-06) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/be8580bc-0eb2-4eb6-a4cc-4ebbeb33424dNADAC price for package 10702007501
GET /v1/drugs/nadac/10702007501
Use it
Look up 10702-075 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/10702-075 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 10702-075. 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.