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OXYMORPHONE HYDROCHLORIDE

NDC 63629-1926, OXYMORPHONE HYDROCHLORIDE, tablet, from Bryant Ranch Prepack.

Product NDC
63629-1926
Status
Listed
Labeler
Bryant Ranch Prepack
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/63629-1926 \
  -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
63629-1926-163629192601100 TABLET in 1 BOTTLE (63629-1926-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/560e9425-dfcb-4fb4-a759-b1e3f8f40fdb

Use it

Look up 63629-1926 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63629-1926 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63629-1926. 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.