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United States· US:68788-8714_8665544f-feee-4577-b765-ec407c6281fb

Megestrol Acetate

A medicinal product containing megestrol acetate, registered in United States by Preferred Pharmaceuticals Inc..

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedMegestrol AcetateATC—REGISTER NO.US:68788-8714_8665544…PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
MEGESTROL ACETATE
Manufacturer
Preferred Pharmaceuticals Inc.
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 1

  • ndc11
    68788-8714-2

Regulatory notes

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

Same medicine, other countries

Megestrol acetate in 14 other countries

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

All megestrol acetate products

Authorised across Europe · EMA

The same active substance is authorised in 22 EEA countries. Names it is sold under:

  • Belgium · Megace
  • Cyprus · Megace
  • Czechia · Megace, Megaplex
  • Germany · Megestat
  • Spain · Borea, Maygace Altas Dosis
  • France · Megace
  • United Kingdom (Northern Ireland) · Megace
  • Greece · Megace
  • Croatia · Megace, Megostat
  • Hungary · Cachexi, Megace
  • Ireland · Megace
  • Italy · Gestroltex, Megace
  • Lithuania · Megace
  • Luxembourg · Megace
  • Netherlands · Megestrolacetaat Focus
  • Norway · Megace
  • Poland · Cachexan, Megace
  • Portugal · Megace, Megestrol Generis
  • Romania · Megesin
  • Sweden · Megace
  • Slovenia · Megace
  • Slovakia · Megesin

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/1b1fecb3-09d6-4e03-904f-39b05c133f91
GET /v1/drugs/1b1fecb3-09d6-4e03-904f-39b05c133f91?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": "40",
  "substance": "MEGESTROL ACETATE",
  "productndc": "68788-8714",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "ANDA075671",
  "marketing_category": "ANDA"
}

See everything about megestrol acetate.

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.