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Dexmethylphenidate Hydrochloride

NDC 0093-5551, Dexmethylphenidate Hydrochloride, capsule, extended release, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-5551
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078908
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-5551 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXMETHYLPHENIDATE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0093-5551-0100093555101100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5551-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd659d39-41f5-4612-8f17-bad602b4784d

  • NADAC price for package 00093555101

    GET /v1/drugs/nadac/00093555101

Use it

Look up 0093-5551 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-5551 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-5551. 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.