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Dexmethylphenidate hydrochloride

NDC 57664-376, Dexmethylphenidate hydrochloride, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-376
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201231
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-376 \
  -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
57664-376-0857664037608100 TABLET in 1 BOTTLE (57664-376-08)
57664-376-1357664037613500 TABLET in 1 BOTTLE (57664-376-13)
57664-376-18576640376181000 TABLET in 1 BOTTLE (57664-376-18)
57664-376-835766403768330 TABLET in 1 BOTTLE (57664-376-83)
57664-376-8857664037688100 TABLET in 1 BOTTLE (57664-376-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/987b4983-1edc-40f1-adc9-724747080969

  • NADAC price for package 57664037688

    GET /v1/drugs/nadac/57664037688

Use it

Look up 57664-376 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-376 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-376. 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.