MedPath

Pectin

Generic Name
Pectin
Brand Names
Luden's Drops, Sucrets
Drug Type
Biotech
CAS Number
9000-69-5
Unique Ingredient Identifier
89NA02M4RX

Overview

Pectin is a heteropolysaccharide commercially derived from the cell wall of higher plants. It is composed of partially methylated polygalacturonic acid units linked in the positions 1-4. The carboxylic group of the constituents of pectin can exist in the form of esters, free acids, ammonium, potassium or sodium salts or as acid amides. Under the FDA regulation, pectin qualifies as a GRAS (generally recognized as safe) food substance. This status allows pectin to be used with no limitations.

Indication

Pectin is used in food as a gelling agent and stabilizer. As a medical drug, it has obtained a great interest in its potential use as a source of dietary fiber, lipid, cholesterol, serum glucose and insulin level lowering effect, gastric emptying delay. Some recent studies have researched the possibility of using pectin for the formation of nanoparticles as a delivery vehicle of drugs.

Associated Conditions

  • Bacterial diarrhoea
  • Diarrhea caused by Salmonella
  • Diarrhea caused by Shigella
  • Diarrhea caused by Staphylococcus
  • Escherichia Coli Diarrhea
  • Sore Throat
  • Mouth soreness

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
BFY LLC
72427-4615
ORAL
11.5 mg in 7 g
5/7/2025
BFY LLC
72427-4014
ORAL
11.5 mg in 3.5 g
5/7/2025
BFY LLC
72427-3295
ORAL
11.5 mg in 7 g
5/7/2025
BFY LLC
72427-3395
ORAL
11.5 mg in 7 g
5/7/2025
BFY LLC
72427-4540
ORAL
11.5 mg in 7 g
5/7/2025
BFY LLC
72427-3195
ORAL
11.5 mg in 7 g
5/7/2025
BFY LLC
72427-3495
ORAL
11.5 mg in 7 g
5/7/2025
BFY LLC
72427-4314
ORAL
11.5 mg in 3.5 g
5/7/2025
BFY LLC
72427-3515
ORAL
11.5 mg in 7 g
5/7/2025
WALGREENS CO.
0363-0492
ORAL
11.5 mg in 1 1
11/5/2024

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
AXCEL KAOPEC SUSPENSION
SIN06496P
SUSPENSION
5 mg/5 ml
8/19/1991
BEAKOPECTIN SUSPENSION
SIN06076P
SUSPENSION
130mg/30ml
5/23/1991

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.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
DIBAN CAP
wyeth-ayerst canada inc.
02041626
Capsule - Oral
71.4 MG
2/18/1998
DIARET TAB
produits francais labs inc.
00540862
Tablet - Oral
45 MG / TAB
12/31/1981
VITAMIN C TAB 600MG
swiss herbal remedies ltd.
00244619
Tablet - Oral
5 MG / TAB
12/31/1972
DONNAGEL LIQ
ayerst laboratories
01908006
Liquid - Oral
142.8 MG / 30 ML
12/31/1993
DONNAGEL-PG LIQ
wyeth-ayerst canada inc.
02041634
Liquid - Oral
142.8 MG / 30 ML
12/31/1994
DIAREX TAB
nutribon (1986) inc.
02003392
Tablet - Oral
45 MG / TAB
12/31/1995
DIBAN CAP
ayerst laboratories
01909215
Capsule - Oral
71.4 MG
12/31/1992
DIARET LIQ
produits francais labs inc.
00540870
Liquid - Oral
150 MG / 30 ML
12/31/1981
KAOLIN MIXTURE W PECTIN NF
stanley pharmaceuticals, a division of vita health products inc.
00238651
Liquid - Oral
10 MG / ML
12/31/1972
WATKINS SETTELZ
watkins incorporated
00373656
Liquid - Oral
274 MG / 28.4 ML
12/31/1954

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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