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Methylphenidate Hydrochloride

NDC 62175-312, Methylphenidate Hydrochloride, tablet, extended release, from Lannett Company, Inc..

Product NDC
62175-312
Status
Listed
Labeler
Lannett Company, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091695
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62175-312 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHYLPHENIDATE HYDROCHLORIDE36 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
62175-312-3762175031237100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-312-37)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3d1f5aff-5d39-496c-b5ed-7f3c70ec641c

  • NADAC price for package 62175031237

    GET /v1/drugs/nadac/62175031237

Use it

Look up 62175-312 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62175-312 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62175-312. 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.