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Methylphenidate Hydrochloride

NDC 72865-136, Methylphenidate Hydrochloride, tablet, extended release, from XLCare Pharmaceuticals, Inc..

Product NDC
72865-136
Status
Listed
Labeler
XLCare Pharmaceuticals, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211009
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72865-136 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPHENIDATE HYDROCHLORIDE54 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72865-136-0172865013601100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-136-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b07150db-fd99-4400-bb83-b3a7544a917a

Use it

Look up 72865-136 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72865-136 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72865-136. 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.