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Mycophenolate Mofetil

NDC 70752-294, Mycophenolate Mofetil, powder, for suspension, from QUAGEN PHARMACEUTICALS LLC.

Product NDC
70752-294
Status
Listed
Labeler
QUAGEN PHARMACEUTICALS LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214525
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70752-294 \
  -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
70752-294-60707520294601 BOTTLE, PLASTIC in 1 CARTON (70752-294-60) / 225 mL in 1 BOTTLE, PLASTIC

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/838449b3-4397-4e35-b9b9-683f5a48bff2

Use it

Look up 70752-294 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70752-294 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70752-294. 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.