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Dexmethylphenidate Hydrochloride

NDC 67877-657, Dexmethylphenidate Hydrochloride, tablet, from Ascend Laboratories, LLC.

Product NDC
67877-657
Status
Listed
Labeler
Ascend Laboratories, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212631
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67877-657 \
  -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
67877-657-0167877065701100 TABLET in 1 BOTTLE (67877-657-01)
67877-657-0567877065705500 TABLET in 1 BOTTLE (67877-657-05)
67877-657-306787706573030 TABLET in 1 BOTTLE (67877-657-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/830df993-db01-40df-beef-90af6b86f561

  • NADAC price for package 67877065701

    GET /v1/drugs/nadac/67877065701

Use it

Look up 67877-657 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-657 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-657. 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.