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Oxymorphone Hydrochloride

NDC 42806-331, Oxymorphone Hydrochloride, tablet, from Epic Pharma, LLC.

Product NDC
42806-331
Status
Listed
Labeler
Epic Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201187
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42806-331 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYMORPHONE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
42806-331-0142806033101100 TABLET in 1 BOTTLE (42806-331-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/95804e72-232d-425d-b23d-a66f43bdf0c6

Use it

Look up 42806-331 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42806-331 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42806-331. 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.