Mycophenolate Mofetil
NDC 66689-307, Mycophenolate Mofetil, powder, for suspension, from VistaPharm, LLC.
- Product NDC
- 66689-307
- Status
- Listed
- Labeler
- VistaPharm, LLC
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210370
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/66689-307 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MYCOPHENOLATE MOFETIL200 mg/mL
Pharmacologic classes
Antimetabolite Immunosuppressant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 66689-307-08 | 66689030708 | 1 BOTTLE, PLASTIC in 1 CARTON (66689-307-08) / 250 mL in 1 BOTTLE, PLASTIC |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/175d8b87-e06a-4c9e-b3de-378114b52274NADAC price for package 66689030708
GET /v1/drugs/nadac/66689030708
Use it
Look up 66689-307 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/66689-307 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 66689-307. 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.