Overview
A local anesthetic of the amide type now generally used for surface anesthesia. It is one of the most potent and toxic of the long-acting local anesthetics and its parenteral use is restricted to spinal anesthesia. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1006)
Indication
适用于硬膜外麻醉以及腰麻。也用于表面麻醉，较少用于浸润麻醉。
Associated Conditions
- Haemorrhoids
- Pruritis of the skin
- Pruritus Ani
- Skin Irritation
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 |
|---|---|---|---|---|---|
| Sincerus Florida, LLC | 72934-5071 | TOPICAL | 0.5 g in 100 g | 5/10/2019 | |
| Pascal Company, Inc. | 10866-0062 | BUCCAL, TOPICAL, DENTAL | 8 mg in 1 g | 12/19/2022 |
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 |
|---|---|---|---|---|---|
| PROCTOSEDYL OINTMENT | SIN01718P | OINTMENT | 0.5% w/w | 6/8/1988 | |
| PROCTOSEDYL SUPPOSITORY | SIN01717P | SUPPOSITORY | 5 mg | 6/8/1988 |
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 |
|---|---|---|---|---|---|
| DECATYLEN LOZ | N/A | N/A | N/A | 3/19/1990 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| SCHERIPROCT prednisolone hexanoate and cinchocaine hydrochloride suppository strip pack | 70063 | Medicine | A | 5/8/2000 | |
| APOHEALTH HAEMORRHOID OINTMENT hydrocortisone 5mg/g and cinchocaine hydrochloride 5mg/g tube | 317870 | Medicine | A | 5/23/2019 | |
| RECTOCAINE hydrocortisone 5mg/g and cinchocaine hydrochloride 5mg/g ointment tube | 317869 | Medicine | A | 5/23/2019 | |
| SCHERIPROCT prednisolone hexanoate and cinchocaine hydrochloride ointment tube | 70062 | Medicine | A | 5/8/2000 | |
| PROCTOSEDYL OINTMENT tube | 21847 | Medicine | A | 6/26/1992 | |
| PROCTOCAINE hydrocortisone 5mg/g and cinchocaine hydrochloride 5mg/g ointment tube | 317868 | Medicine | A | 5/23/2019 | |
| PROCTOSEDYL SUPPOSITORIES strip pack | 22614 | Medicine | A | 6/26/1992 | |
| RECTINOL HAEMORRHOIDAL ointment tube | 119786 | Medicine | A | 6/9/2005 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| PROCTOSEDYL OINTMENT | hoechst roussel canada inc. | 01988549 | Ointment - Rectal | 5 MG / G | 12/31/1971 |
| NUPERCAINAL ANESTHETIC OINTMENT 1% | glaxosmithkline consumer healthcare ulc | 00623385 | Ointment - Topical
,
Rectal | 1 % | 12/31/1944 |
| TEVA-PROCTOSONE | teva canada limited | 02226391 | Suppository - Rectal | 5 MG | 12/30/1996 |
| PROCTOSEDYL | Aptalis Pharma Canada ULC | 02223252 | Ointment - Rectal | 0.5 % | 4/1/2003 |
| PROCTOSEDYL SUP | roussel canada inc. | 00173622 | Suppository - Rectal | 5 MG | 12/31/1959 |
| PROCTOSONE ONT | technilab pharma inc. | 00530093 | Ointment - Rectal | .5 % | 12/31/1981 |
| ODAN PROCTOMYXIN HC | odan laboratories ltd | 02242527 | Ointment - Rectal | 0.5 % | 3/9/2001 |
| TRUE TEST | 02271885 | Patch - Topical | 0.073 MG | 3/16/2006 | |
| PROCTOL SUPPOSITORIES | odan laboratories ltd | 02247882 | Suppository - Rectal | 5 MG | 3/15/2004 |
| PROCTOSONE SUP | technilab pharma inc. | 00530085 | Suppository - Rectal | 5 MG / SUP | 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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