oxycodone hydrochloride and acetaminophen
NDC 72887-648, oxycodone hydrochloride and acetaminophen, solution, from FH2 Pharma LLC.
- Product NDC
- 72887-648
- Status
- Listed
- Labeler
- FH2 Pharma LLC
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202142
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/72887-648 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OXYCODONE HYDROCHLORIDE10 mg/5mL
- ACETAMINOPHEN300 mg/5mL
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72887-648-12 | 72887064812 | 120 mL in 1 BOTTLE, PLASTIC (72887-648-12) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/96b0067e-aabe-df4f-e053-2995a90a4a86
Use it
Look up 72887-648 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72887-648 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72887-648. 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.