MYLERAN
NDC 80725-620, busulfan, tablet, film coated, from Waylis Therapeutics LLC.
- Product NDC
- 80725-620
- Status
- Listed
- Labeler
- Waylis Therapeutics LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA009386
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/80725-620 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUSULFAN2 mg/1
Pharmacologic classes
Alkylating Activity [MoA]; Alkylating Drug [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 80725-620-25 | 80725062025 | 25 TABLET, FILM COATED in 1 BOTTLE (80725-620-25) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2da33e5b-dcfb-4cdf-b163-50398e42f41c
Use it
Look up 80725-620 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80725-620 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80725-620. 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.