OXYCODONE AND ACETAMINOPHEN
NDC 10702-238, oxycodone and acetaminophen, solution, from KVK-Tech, Inc..
- Product NDC
- 10702-238
- Status
- Listed
- Labeler
- KVK-Tech, Inc.
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211499
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/10702-238 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OXYCODONE HYDROCHLORIDE5 mg/5mL
- ACETAMINOPHEN325 mg/5mL
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 10702-238-50 | 10702023850 | 500 mL in 1 BOTTLE (10702-238-50) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/9986aa04-c976-4654-8ad7-b97d2eecea93
Use it
Look up 10702-238 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/10702-238 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 10702-238. 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.