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United States· US:0904-7372_7a9902d5-629e-4ed5-8747-715b3a582556

MYCOPHENOLIC ACID

A medicinal product containing mycophenolate sodium, registered in United States by Major Pharmaceuticals.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedMYCOPHENOLIC ACIDATC—REGISTER NO.US:0904-7372_7a9902d5…PACKS LISTED4CHECKEDJuly 12, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about mycophenolate sodiumAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
MYCOPHENOLATE SODIUM
Manufacturer
Major Pharmaceuticals
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
July 12, 2026

Packs & prices · 4

  • ndc11
    0904-7372-04
  • ndc11
    0904-7372-61
  • ndc11
    0904737204
    30 BLISTER PACK in 1 CARTON (0904-7372-04) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
  • ndc11
    0904737261
    100 BLISTER PACK in 1 CARTON (0904-7372-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Mycophenolate sodium in 5 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All mycophenolate sodium products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • Germany · Mycophenolsäure Hexal
  • Spain · Ceptava
  • Italy · Ceptava
  • Portugal · Ácido Micofenólico Accord

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/d1d62df2-37b6-480e-b574-3c99c9263ec0
GET /v1/drugs/d1d62df2-37b6-480e-b574-3c99c9263ec0?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "360",
  "substance": "MYCOPHENOLATE SODIUM",
  "productndc": "0904-7372",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "ANDA208315",
  "marketing_category": "ANDA"
}
API referenceMCP serverPlans

See everything about mycophenolate sodium.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.

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