United States· US:63545-495_de0f84f3-5f8a-2ac2-e053-2995a90a8caa
Bismuthum Subnitricum
A bismuth subnitrate product containing bismuth subnitrate, registered in United States by Hahnemann Laboratories, INC.. The same ATC class is registered in 3 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Bismuth subnitrate is registered in 3 of 19 countries.
Countries holding a registration under ATC A02BX12 (bismuth subnitrate), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 1 of them publish a price we can compare per daily dose
Bismuth subnitrate · ATC A02BX12
3 / 19 countries
- Japan
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- BISMUTH SUBNITRATE
- Manufacturer
- Hahnemann Laboratories, INC.
- Country
- United States (US)
- ATC code
- A02BX12
- ATC class
- Bismuth subnitrate
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 8
- ndc1163545-495-03
- ndc1163545-495-01
- ndc1163545-495-02
- ndc1163545-495-04
- ndc116354549501200 PELLET in 1 VIAL, GLASS (63545-495-01)
- ndc116354549502500 PELLET in 1 VIAL, GLASS (63545-495-02)
- ndc1163545495033000 PELLET in 1 BOTTLE, GLASS (63545-495-03)
- ndc11635454950410000 PELLET in 1 BOTTLE, GLASS (63545-495-04)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Bismuth subnitrate in 2 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- France · Bismuth Granions
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/d575d18e-c4df-41ca-b72f-c9077de630a1 GET /v1/drugs/d575d18e-c4df-41ca-b72f-c9077de630a1?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": "200",
"substance": "BISMUTH SUBNITRATE",
"productndc": "63545-495",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about bismuth subnitrate.
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.