Hydromorphone Hydrochloride
NDC 42858-303, Hydromorphone Hydrochloride, tablet, from Rhodes Pharmaceuticals LLC.
- Product NDC
- 42858-303
- Status
- Listed
- Labeler
- Rhodes Pharmaceuticals LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA019892
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/42858-303 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROMORPHONE HYDROCHLORIDE8 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42858-303-01 | 42858030301 | 100 TABLET in 1 BOTTLE, PLASTIC (42858-303-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/37565441-0d95-4743-a695-d7b3326f58a1NADAC price for package 42858030301
GET /v1/drugs/nadac/42858030301
Use it
Look up 42858-303 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42858-303 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42858-303. 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.