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Methylphenidate Hydrochloride

NDC 10702-102, Methylphenidate Hydrochloride, tablet, from KVK-TECH, INC..

Product NDC
10702-102
Status
Listed
Labeler
KVK-TECH, INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206932
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10702-102 \
  -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 NDCNDC-11Package
10702-102-0110702010201100 TABLET in 1 BOTTLE (10702-102-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1bf37f9f-29cf-4b09-9c81-eb369e35a042

  • NADAC price for package 10702010201

    GET /v1/drugs/nadac/10702010201

Use it

Look up 10702-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-102. 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.