Ifosfamide
NDC 21586-211, Ifosfamide for Injection, powder, for solution, from SteriMax Inc..
- Product NDC
- 21586-211
- Status
- Listed
- Labeler
- SteriMax Inc.
- Dosage form
- POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/21586-211 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- IFOSFAMIDE1 g/1
Pharmacologic classes
Alkylating Activity [MoA]; Alkylating Drug [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 21586-211-02 | 21586021102 | 5 VIAL in 1 CARTON (21586-211-02) / 1 POWDER, FOR SOLUTION in 1 VIAL (21586-211-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/98798c5e-8384-4990-a1b5-60dfb1e667bb
Use it
Look up 21586-211 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/21586-211 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 21586-211. 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.