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NDC 0004-0261, Mycophenolate Mofetil, powder, for suspension, from Genentech, Inc..

Product NDC
0004-0261
Status
Listed
Labeler
Genentech, Inc.
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA050759
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0004-0261 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MYCOPHENOLATE MOFETIL200 mg/mL

Pharmacologic classes

Antimetabolite Immunosuppressant [EPC]

Package NDCNDC-11Package
0004-0261-29000040261291 BOTTLE, PLASTIC in 1 CARTON (0004-0261-29) / 225 mL in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/37241e87-4af4-4dc3-a1aa-ea6f20d8dc40

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0004-0261

  • NADAC price for package 00004026129

    GET /v1/drugs/nadac/00004026129

Use it

Look up 0004-0261 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0004-0261 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0004-0261. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.