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hydromorphone hydrochloride

NDC 31722-122, hydromorphone hydrochloride, tablet, extended release, from Camber Pharmaceuticals, Inc..

Product NDC
31722-122
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212133
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-122 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROMORPHONE HYDROCHLORIDE32 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
31722-122-0131722012201100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-122-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c33e6320-4206-4b69-8cac-ebfc2351b8f2

Use it

Look up 31722-122 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-122 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-122. 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.