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Methylphenidate Hydrochloride

NDC 57664-230, Methylphenidate Hydrochloride, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-230
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090710
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-230 \
  -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
57664-230-0857664023008100 TABLET in 1 BOTTLE (57664-230-08)
57664-230-1357664023013500 TABLET in 1 BOTTLE (57664-230-13)
57664-230-18576640230181000 TABLET in 1 BOTTLE (57664-230-18)
57664-230-835766402308330 TABLET in 1 BOTTLE (57664-230-83)
57664-230-8857664023088100 TABLET in 1 BOTTLE (57664-230-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1a89b390-0cd5-45cb-9e70-20de44652c56

  • NADAC price for package 57664023088

    GET /v1/drugs/nadac/57664023088

Use it

Look up 57664-230 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-230. 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.