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Mycophenolate mofetil

NDC 67877-230, Mycophenolate mofetil, powder, for suspension, from Ascend Laboratories, LLC.

Product NDC
67877-230
Status
Listed
Labeler
Ascend Laboratories, LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203005
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67877-230 \
  -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
67877-230-22678770230221 BOTTLE, PLASTIC in 1 CARTON (67877-230-22) / 225 mL in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/21ff53b0-b4ba-4473-91e4-76ef41681064

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=67877-230

  • NADAC price for package 67877023022

    GET /v1/drugs/nadac/67877023022

Use it

Look up 67877-230 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-230. 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.