Mycophenolate Mofetil
NDC 54288-141, Mycophenolate Mofetil hydrochloride, injection, powder, lyophilized, for solution, from BPI Labs LLC.
- Product NDC
- 54288-141
- Status
- Listed
- Labeler
- BPI Labs LLC
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214283
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/54288-141 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MYCOPHENOLATE MOFETIL HYDROCHLORIDE500 mg/20mL
Pharmacologic classes
Antimetabolite Immunosuppressant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 54288-141-04 | 54288014104 | 4 VIAL in 1 CARTON (54288-141-04) / 20 mL in 1 VIAL |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/32001417-130d-4c08-8e63-94ba3627ce5f
Use it
Look up 54288-141 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/54288-141 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 54288-141. 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.