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Oxymorphone Hydrochloride

NDC 10702-070, Oxymorphone Hydrochloride, tablet, from KVK-Tech, Inc..

Product NDC
10702-070
Status
Listed
Labeler
KVK-Tech, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203601
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10702-070 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYMORPHONE HYDROCHLORIDE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
10702-070-0110702007001100 TABLET in 1 BOTTLE (10702-070-01)
10702-070-061070200700660 TABLET in 1 BOTTLE (10702-070-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dcb5b5d2-7d0a-497a-8f1e-3b96fd43320b

Use it

Look up 10702-070 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-070 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-070. 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.