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MYCOPHENOLATE MOFETIL

NDC 72603-751, mycophenolate mofetil, powder, for suspension, from NorthStar Rx LLC.

Product NDC
72603-751
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218227
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72603-751 \
  -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
72603-751-01726030751011 BOTTLE in 1 CARTON (72603-751-01) / 225 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/127eabe2-8386-452a-ad6b-d879e1f2c099

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=72603-751

  • NADAC price for package 72603075101

    GET /v1/drugs/nadac/72603075101

Use it

Look up 72603-751 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-751 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-751. 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.