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NDC 0004-0298, Mycophenolate Mofetil hydrochloride, injection, powder, lyophilized, for solution, from Genentech, Inc..

Product NDC
0004-0298
Status
Listed
Labeler
Genentech, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA050758
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0004-0298 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MYCOPHENOLATE MOFETIL HYDROCHLORIDE500 mg/20mL

Pharmacologic classes

Antimetabolite Immunosuppressant [EPC]

Package NDCNDC-11Package
0004-0298-09000040298094 VIAL in 1 CARTON (0004-0298-09) / 20 mL in 1 VIAL

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=0004-0298

Use it

Look up 0004-0298 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0004-0298 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0004-0298. 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.