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OXYMORPHONE HYDROCHLORIDE

NDC 31722-930, OXYMORPHONE HYDROCHLORIDE, tablet, from Camber Pharmaceuticals, Inc.

Product NDC
31722-930
Status
Listed
Labeler
Camber Pharmaceuticals, Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210175
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-930 \
  -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
31722-930-0131722093001100 TABLET in 1 BOTTLE (31722-930-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/06af7dff-c261-4c03-9cd9-0605c42507fa

Use it

Look up 31722-930 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-930 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-930. 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.