Overview
Bismuth subnitrate, also referred to as bismuth oxynitrate or bismuthyl nitrate, is a highly water-soluble crystalline compound that has been used as a treatment for duodenal ulcers and anti-diarrheic agent . The use of bismuth substrate as an active ingredient in over-the-counter antacids is approved by the FDA.
Indication
主要用于消化性溃疡、腹泻、肠炎等。
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| No FDA approvals found for this drug. | |||||
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No HSA approvals found for this drug. | |||||
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| ROTER TAB | N/A | N/A | N/A | 10/23/2001 | |
| SPAGASTROL TAB | N/A | N/A | N/A | 3/5/1987 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| ROTER TABLETS | roter pharmaceutische fabriek | 00173797 | Tablet - Oral | 350 MG | 12/31/1952 |
| BISMUTUM SUBNITRICUM-INJEEL LIQ (12D,30D,200D/1.1ML) | 02062496 | Liquid - Oral | 12 D / 1.1 ML | 12/31/1994 | |
| BISMUTHUM SUBNITRICUM | dolisos canada inc. | 02234352 | Liquid
,
Globules
,
Granules - Oral | 6 X | 1/5/1998 |
| BISMUTUM SUBNITRICUM-INJEEL FORTE LIQ (6D,12D,30D,200D/1.1ML) | 02066262 | Liquid - Oral | 6 D / 1.1 ML | 12/31/1994 | |
| HEMORRO-DOL SUP | produits francais labs inc. | 00540919 | Suppository - Rectal | 37.8 MG / SUP | 12/31/1981 |
| HEMORRO-DOL ONT | produits francais labs inc. | 00540900 | Ointment - Rectal | 1.5 % | 12/31/1981 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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