OJEMDA
NDC 82950-001, TOVORAFENIB, tablet, film coated, from Day One Biopharmaceuticals, Inc..
- Product NDC
- 82950-001
- Status
- Listed
- Labeler
- Day One Biopharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA217700
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/82950-001 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TOVORAFENIB100 mg/1
Pharmacologic classes
Cytochrome P450 3A Inducers [MoA]; Kinase Inhibitor [EPC]; Type II RAF Kinase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 82950-001-16 | 82950000116 | 4 BLISTER PACK in 1 CARTON (82950-001-16) / 4 TABLET, FILM COATED in 1 BLISTER PACK (82950-001-04) |
| 82950-001-20 | 82950000120 | 4 BLISTER PACK in 1 CARTON (82950-001-20) / 5 TABLET, FILM COATED in 1 BLISTER PACK (82950-001-05) |
| 82950-001-24 | 82950000124 | 4 BLISTER PACK in 1 CARTON (82950-001-24) / 6 TABLET, FILM COATED in 1 BLISTER PACK (82950-001-06) |
Linked data
RxNorm, label and prices
RxNorm concepts
- 2690858{16 (tovorafenib 100 MG Oral Tablet [Ojemda]) } Pack [Ojemda 400 MG Once Weekly Carton] (BPCK)
- 2690860{20 (tovorafenib 100 MG Oral Tablet [Ojemda]) } Pack [Ojemda 500 MG Once Weekly Carton] (BPCK)
- 2690862{24 (tovorafenib 100 MG Oral Tablet [Ojemda]) } Pack [Ojemda 600 MG Once Weekly Carton] (BPCK)
Related lookups
FDA label sections
GET /v1/drugs/labels/ea3a9631-3a66-6a7c-e053-2995a90ae2ad
Use it
Look up 82950-001 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82950-001 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82950-001. 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.