United States· US:65162-842_8fcab8b3-47d1-4172-bd8e-7e89fe6daa25
Lubiprostone
A lubiprostone product containing lubiprostone, registered in United States by Amneal Pharmaceuticals LLC. The same ATC class is registered in 4 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Lubiprostone is registered in 4 of 19 countries.
Countries holding a registration under ATC A06AX03 (lubiprostone), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 2 of them publish a price we can compare per daily dose
Lubiprostone · ATC A06AX03
4 / 19 countries
- Belgiumprice
- Japan
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- LUBIPROSTONE
- Manufacturer
- Amneal Pharmaceuticals LLC
- Country
- United States (US)
- ATC code
- A06AX03
- ATC class
- Lubiprostone
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1165162-842-06
- ndc1165162-842-18
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
2 interactions on record for lubiprostone.
Graded by severity as the source publishes them — 2 moderate. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Lubiprostone · interactions on record
2 records
- 2 moderate
Most severe, free to view
- IdelalisibL01EM01moderate
- IdelalisibL01XX47moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Lubiprostone in 2 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
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/0c541dcd-07d0-4b87-9d37-6d48523e15b3 GET /v1/drugs/0c541dcd-07d0-4b87-9d37-6d48523e15b3?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": "24",
"substance": "LUBIPROSTONE",
"productndc": "65162-842",
"dosage_form": "CAPSULE",
"dea_schedule": null,
"strength_unit": "ug/1",
"application_number": "ANDA209450",
"marketing_category": "ANDA"
}See everything about lubiprostone.
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.