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Chlorpropamide

Generic Name
Chlorpropamide
Drug Type
Small Molecule
Chemical Formula
C10H13ClN2O3S
CAS Number
94-20-2
Unique Ingredient Identifier
WTM2C3IL2X

Overview

Chlorpropamide is an oral antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus (NIDDM). It belongs to the sulfonylurea class of insulin secretagogues, which act by stimulating β cells of the pancreas to release insulin. Sulfonylureas increase both basal insulin secretion and meal-stimulated insulin release. Medications in this class differ in their dose, rate of absorption, duration of action, route of elimination and binding site on their target pancreatic β cell receptor. Sulfonylureas also increase peripheral glucose utilization, decrease hepatic gluconeogenesis and may increase the number and sensitivity of insulin receptors. Sulfonylureas are associated with weight gain, though less so than insulin. Due to their mechanism of action, sulfonylureas may cause hypoglycemia and require consistent food intake to decrease this risk. The risk of hypoglycemia is increased in elderly, debilitated and malnourished individuals. Chlorpropamide is not recommended for the treatment of NIDDM as it increases blood pressure and the risk of retinopathy (UKPDS-33). Up to 80% of the single oral dose of chlorpropramide is metabolized, likely in the liver; 80-90% of the dose is excreted in urine as unchanged drug and metabolites. Renal and hepatic dysfunction may increase the risk of hypoglycemia.

Indication

For treatment of NIDDM in conjunction with diet and exercise.

Associated Conditions

  • Diabetes Insipidus
  • Type 2 Diabetes Mellitus

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
1999/10/19
N/A
Completed
National Center for Research Resources (NCRR)

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
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
CHLORPROPAMIDE TAB 250MG
00430986
Tablet - Oral
250 MG
12/31/1978
NOVO-PROPAMIDE 250MG
novopharm limited
00021350
Tablet - Oral
250 MG
12/31/1969
CHLORPROPAMIDE 100 TAB USP
PRO DOC LIMITEE
00586773
Tablet - Oral
100 MG
12/31/1983
DIABINESE TAB 100MG
00024708
Tablet - Oral
100 MG / TAB
12/31/1958
DIABINESE TAB 250MG
00024716
Tablet - Oral
250 MG / TAB
12/31/1958
APO CHLORPROPAMIDE TAB 100MG
00399302
Tablet - Oral
100 MG
12/31/1977
CHLORPROPAMIDE TAB 250MG
PRO DOC LIMITEE
00156728
Tablet - Oral
250 MG
12/31/1969
APO CHLORPROPAMIDE TAB 250MG
00312711
Tablet - Oral
250 MG
12/31/1974

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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