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Methylphenidate Hydrochloride

NDC 13107-381, Methylphenidate Hydrochloride, tablet, from Aurolife Pharma, LLC.

Product NDC
13107-381
Status
Listed
Labeler
Aurolife Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209276
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/13107-381 \
  -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
13107-381-0113107038101100 TABLET in 1 BOTTLE (13107-381-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/35be77db-fbe3-487e-a220-a08a11aaec28

Use it

Look up 13107-381 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/13107-381 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 13107-381. 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.