Pemfexy
NDC 71390-250, pemetrexed, injection, from Acacia Pharma, Ltd..
- Product NDC
- 71390-250
- Status
- Listed
- Labeler
- Acacia Pharma, Ltd.
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA209472
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71390-250 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PEMETREXED MONOHYDRATE25 mg/mL
Pharmacologic classes
Folate Analog Metabolic Inhibitor [EPC]; Folic Acid Metabolism Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71390-250-02 | 71390025002 | 1 VIAL in 1 CARTON (71390-250-02) / 20 mL in 1 VIAL |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/caef07ce-066b-4c48-98dc-974b05ebbbe0Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=71390-250
Use it
Look up 71390-250 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71390-250 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71390-250. 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.