MedPath

Paraformaldehyde

Generic Name
Paraformaldehyde

Overview

No overview information available.

Indication

口腔科应用甚广。高浓度多聚甲醛作为牙髓失活剂,作用缓慢且安全,封药时间2周左右,封药时间延长或药物漏出均无大的影响,因此适用于乳牙。低浓度多聚甲醛间接盖髓,但残留的牙本质厚度应在1mm以上,才能获得满意效果,如残留牙本质较薄,易诱发牙髓炎。还可作为牙髓干髓剂、根管充填剂、抗牙本质敏感剂的主要药物。

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

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Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

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Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

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Approval Number
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Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

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Company
Approval Number
Drug Type
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Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

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Registration No.
Company
Licence No.
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Registration Date
No PPB approvals found for this drug.

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
PT POWDER PT LIQUID 1 PT LIQUID 2
coralite dental products
00070262
Powder For Solution ,  Liquid - Dental
2 %
1/19/1993
ENDOMETHASONE IVORY
00229679
Powder - Dental
2.2 G / 100 G
12/31/1972
CAUSTINERF
00229644
Tablet - Dental
2.16 MG / TAB
12/31/1972

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

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Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

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License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

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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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