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mycophenolate mofetil

NDC 83270-000, mycophenolate mofetil, injection, powder, lyophilized, for solution, from ONESOURCE SPECIALTY PHARMA LIMITED.

Product NDC
83270-000
Status
Listed
Labeler
ONESOURCE SPECIALTY PHARMA LIMITED
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216390
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/83270-000 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MYCOPHENOLATE MOFETIL500 mg/20mL

Pharmacologic classes

Antimetabolite Immunosuppressant [EPC]

Package NDCNDC-11Package
83270-000-04832700000044 VIAL in 1 CARTON (83270-000-04) / 20 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/461a252f-ff81-4e08-b256-a497b14835fa

Use it

Look up 83270-000 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83270-000 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83270-000. 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.