MAYZENT
NDC 0078-0979, siponimod, tablet, film coated, from Novartis Pharmaceuticals Corporation.
- Product NDC
- 0078-0979
- Status
- Listed
- Labeler
- Novartis Pharmaceuticals Corporation
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA209884
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0078-0979 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SIPONIMOD.25 mg/1
Pharmacologic classes
Sphingosine 1-Phosphate Receptor Modulators [MoA]; Sphingosine 1-phosphate Receptor Modulator [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0078-0979-12 | 00078097912 | 12 TABLET, FILM COATED in 1 BLISTER PACK (0078-0979-12) |
| 0078-0979-50 | 00078097950 | 28 TABLET, FILM COATED in 1 BOTTLE (0078-0979-50) |
| 0078-0979-89 | 00078097989 | 7 TABLET, FILM COATED in 1 BLISTER PACK (0078-0979-89) |
| 0078-0979-92 | 00078097992 | 28 TABLET, FILM COATED in 1 BOTTLE (0078-0979-92) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/44492772-5aed-4627-bd85-e8e89f308bb3
Use it
Look up 0078-0979 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0078-0979 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0078-0979. 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.