Mycophenolate mofetil
NDC 42543-989, Mycophenolate mofetil, tablet, film coated, from Strides Pharma Inc..
- Product NDC
- 42543-989
- Status
- Listed
- Labeler
- Strides Pharma Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090456
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42543-989 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MYCOPHENOLATE MOFETIL500 mg/1
Pharmacologic classes
Antimetabolite Immunosuppressant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42543-989-07 | 42543098907 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42543-989-07) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9d8c09fc-1df2-4f39-8e1a-c4b296d1a260
Use it
Look up 42543-989 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42543-989 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42543-989. 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.