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Mycophenolate Mofetil

NDC 31722-879, Mycophenolate Mofetil, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-879
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208119
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-879 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MYCOPHENOLATE MOFETIL500 mg/1

Pharmacologic classes

Antimetabolite Immunosuppressant [EPC]

Package NDCNDC-11Package
31722-879-0131722087901100 TABLET, FILM COATED in 1 BOTTLE (31722-879-01)
31722-879-0531722087905500 TABLET, FILM COATED in 1 BOTTLE (31722-879-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c3ded171-89da-4644-9ee8-dbcf6258036f
  • NADAC price for package 31722087901

    GET /v1/drugs/nadac/31722087901
  • NADAC price for package 31722087905

    GET /v1/drugs/nadac/31722087905

Use it

Look up 31722-879 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-879 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-879. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.