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Methylphenidate Hydrochloride

NDC 67877-617, Methylphenidate Hydrochloride, tablet, from Ascend Laboratories, LLC.

Product NDC
67877-617
Status
Listed
Labeler
Ascend Laboratories, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211779
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67877-617 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPHENIDATE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
67877-617-0167877061701100 TABLET in 1 BOTTLE (67877-617-01)
67877-617-336787706173310 BLISTER PACK in 1 CARTON (67877-617-33) / 1 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8e97c9f3-956c-416a-a7c2-68bb92053ce5

  • NADAC price for package 67877061701

    GET /v1/drugs/nadac/67877061701

Use it

Look up 67877-617 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-617 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-617. 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.