Oxymorphone hydrochloride
NDC 64896-695, Oxymorphone hydrochloride, tablet, film coated, extended release, from Amneal Pharmaceuticals LLC.
- Product NDC
- 64896-695
- Status
- Listed
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA079087
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/64896-695 \ -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 |
|---|---|---|
| 64896-695-01 | 64896069501 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-01) |
| 64896-695-03 | 64896069503 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-03) |
| 64896-695-08 | 64896069508 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-08) |
| 64896-695-13 | 64896069513 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-695-13) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/3f4e703a-e398-42fd-8759-e398c79955f1
Use it
Look up 64896-695 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/64896-695 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 64896-695. 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.