PEMRYDI RTU
NDC 70121-2462, Pemetrexed disodium, injection, from Amneal Pharmaceuticals LLC.
- Product NDC
- 70121-2462
- Status
- Listed
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA215179
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70121-2462 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PEMETREXED DISODIUM HEMIPENTAHYDRATE1000 mg/100mL
Pharmacologic classes
Folate Analog Metabolic Inhibitor [EPC]; Folic Acid Metabolism Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70121-2462-1 | 70121246201 | 1 VIAL in 1 CARTON (70121-2462-1) / 100 mL in 1 VIAL |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/0f006b06-ab85-423d-ba0c-dfc3fc25844e
Use it
Look up 70121-2462 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70121-2462 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70121-2462. 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.