Ondansetron Hydrochloride
NDC 85509-1076, Ondansetron Hydrochloride, tablet, film coated, from PHOENIX RX LLC.
- Product NDC
- 85509-1076
- Status
- Listed
- Labeler
- PHOENIX RX LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078539
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1076 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ONDANSETRON HYDROCHLORIDE8 mg/1
Pharmacologic classes
Serotonin 3 Receptor Antagonists [MoA]; Serotonin-3 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 85509-1076-1 | 85509107601 | 10 TABLET, FILM COATED in 1 BOTTLE (85509-1076-1) |
| 85509-1076-2 | 85509107602 | 20 TABLET, FILM COATED in 1 BOTTLE (85509-1076-2) |
| 85509-1076-3 | 85509107603 | 30 TABLET, FILM COATED in 1 BOTTLE (85509-1076-3) |
| 85509-1076-5 | 85509107605 | 15 TABLET, FILM COATED in 1 BOTTLE (85509-1076-5) |
| 85509-1076-6 | 85509107606 | 60 TABLET, FILM COATED in 1 BOTTLE (85509-1076-6) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3a76bae2-04c2-ee2d-e063-6394a90ad4c8
Use it
Look up 85509-1076 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1076 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 85509-1076. 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.