Ondansetron
NDC 0121-4882, Ondansetron, solution, from PAI Holdings, LLC dba PAI Pharma.
- Product NDC
- 0121-4882
- Status
- Listed
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078127
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0121-4882 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ONDANSETRON HYDROCHLORIDE4 mg/5mL
Pharmacologic classes
Serotonin 3 Receptor Antagonists [MoA]; Serotonin-3 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0121-4882-94 | 00121488294 | 3 TRAY in 1 CASE (0121-4882-94) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (0121-4882-05) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/68a4d845-0c1c-4867-bfca-c0fb11dc93cd
Use it
Look up 0121-4882 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0121-4882 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0121-4882. 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.