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Dexmethylphenidate Hydrochloride Extended-Release

NDC 0527-8109, dexmethylphenidate hydrochloride, capsule, extended release, from Lannett Company, Inc..

Product NDC
0527-8109
Status
Listed
Labeler
Lannett Company, Inc.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210279
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0527-8109 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXMETHYLPHENIDATE HYDROCHLORIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0527-8109-3700527810937100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-8109-37)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/edad7c67-a872-41ad-a8bd-169278693cc2

  • NADAC price for package 00527810937

    GET /v1/drugs/nadac/00527810937

Use it

Look up 0527-8109 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0527-8109 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0527-8109. 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.