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Oxycodone Hydrochloride

NDC 13107-057, Oxycodone Hydrochloride, tablet, from Aurolife Pharma, LLC.

Product NDC
13107-057
Status
Listed
Labeler
Aurolife Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202160
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/13107-057 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYCODONE HYDROCHLORIDE30 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA]; Opioid Agonist [EPC]

Package NDCNDC-11Package
13107-057-0113107005701100 TABLET in 1 BOTTLE (13107-057-01)
13107-057-301310700573030 TABLET in 1 BOTTLE (13107-057-30)
13107-057-99131070057991000 TABLET in 1 BOTTLE (13107-057-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/96ad4352-fff3-46a7-85de-466cc161045e

  • NADAC price for package 13107005701

    GET /v1/drugs/nadac/13107005701

Use it

Look up 13107-057 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/13107-057 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 13107-057. 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.