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Methylphenidate Hydrochloride

NDC 57664-710, Methylphenidate Hydrochloride, tablet, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-710
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217229
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-710 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPHENIDATE HYDROCHLORIDE72 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
57664-710-835766407108330 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-83)
57664-710-8857664071088100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/18024571-4505-6d51-e063-6294a90a1972

  • NADAC price for package 57664071083

    GET /v1/drugs/nadac/57664071083

Use it

Look up 57664-710 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-710 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-710. 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.