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Dexmethylphenidate Hydrochloride

NDC 10702-106, Dexmethylphenidate Hydrochloride, tablet, from KVK-TECH, INC.

Product NDC
10702-106
Status
Listed
Labeler
KVK-TECH, INC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206931
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10702-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXMETHYLPHENIDATE HYDROCHLORIDE2.5 mg/1

Pharmacologic classes

Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]

Package NDCNDC-11Package
10702-106-0110702010601100 TABLET in 1 BOTTLE (10702-106-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0c717ae4-ec27-47db-ac1b-e504dbb379be

  • NADAC price for package 10702010601

    GET /v1/drugs/nadac/10702010601

Use it

Look up 10702-106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-106. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.