OXYMORPHONE HYDROCHLORIDE
NDC 31722-929, OXYMORPHONE HYDROCHLORIDE, tablet, from Camber Pharmaceuticals, Inc.
- Product NDC
- 31722-929
- Status
- Listed
- Labeler
- Camber Pharmaceuticals, Inc
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210175
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/31722-929 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 31722-929-01 | 31722092901 | 100 TABLET in 1 BOTTLE (31722-929-01) |
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 31722-929 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/31722-929 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 31722-929. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.