Hydromorphone Hydrochloride
NDC 60687-590, hydromorphone hydrochloride, tablet, from American Health Packaging.
- Product NDC
- 60687-590
- Status
- Listed
- Labeler
- American Health Packaging
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076855
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/60687-590 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROMORPHONE HYDROCHLORIDE4 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60687-590-01 | 60687059001 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-590-01) / 1 TABLET in 1 BLISTER PACK (60687-590-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e4758743-9b2c-4612-8399-ad2db372e2b7NADAC price for package 60687059001
GET /v1/drugs/nadac/60687059001
Use it
Look up 60687-590 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-590 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-590. 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.