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Oxymorphone Hydrochloride

NDC 0054-0284, oxymorphone hydrochloride, tablet, from Hikma Pharmaceuticals USA Inc..

Product NDC
0054-0284
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090964
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0054-0284 \
  -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
0054-0284-2500054028425100 TABLET in 1 BOTTLE (0054-0284-25)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3eb971cf-ab82-49f3-a46c-4d76a8ce599e

Use it

Look up 0054-0284 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0054-0284 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0054-0284. 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.