Registered Rwanda · Rwanda FDA

TENGLYN

TENELIGLIPTIN

Rwanda FDA-HMP-MA-2302 TABLETS 20 mg

What it does

Teneligliptin is a medication used to help control blood sugar levels in people with diabetes.

Commonly used for: type 2 diabetes, non-insulin dependent diabetes mellitus

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
Rwanda FDA-HMP-MA-2302
Registration date
12/05/2025
Expiry date
11/05/2030
Status
Registered
Active ingredient
TENELIGLIPTIN
Dosage form
TABLETS
Strength
20 mg
Pack size
3x10 Tablets
Therapeutic class
-
Manufacturer / MAH
Zydus Lifesciences
Applicant / LTR
ZYDUS LIFESCIENCES LIMITED
Country of origin
INDIA
Manufacturer location
Sarkhej-Bavla Rd, Sarkhej, Ahmedabad, Changodar, Gujarat 382213, India

Source: Rwanda Food and Drugs Authority · fetched 2026-03-11 22:07:03 · updated 2026-09-17 02:30:42

Disclaimer: This information is sourced from Rwanda Food and Drugs Authority (Rwanda). Always consult a qualified healthcare professional before using any medication.

About this medicine

Teneligliptin is a medication used to help control blood sugar levels in people with diabetes.

What it treats

  • type 2 diabetes
  • non-insulin dependent diabetes mellitus

How it works

It works by increasing the levels of hormones that help regulate blood sugar, leading to better control of glucose levels in the blood.

Who it's for

This medication is for adults with type 2 diabetes who need help managing their blood sugar levels.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: teneligliptin

BNF-referenced

Teneligliptin is an oral hypoglycemic agent belonging to the dipeptidyl peptidase-4 (DPP-4) inhibitors class. It is primarily used in the management of type 2 diabetes mellitus, as it helps to lower blood glucose levels by increasing insulin secretion and decreasing glucagon secretion in a glucose-dependent manner. This drug is particularly beneficial for patients who require additional glycemic control beyond diet and exercise alone.

Indications

  • Type 2 diabetes mellitus
  • Hyperglycemia in adults with type 2 diabetes

Dosage

Adults: The usual recommended dose of teneligliptin is 20 mg once daily, taken orally. In patients with renal impairment, dose adjustments may be required according to renal function.

Mechanism of action

Teneligliptin inhibits the enzyme DPP-4, which is responsible for the degradation of incretin hormones, such as glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP). By inhibiting DPP-4, teneligliptin increases the levels of these incretins, leading to enhanced insulin secretion from the pancreatic beta cells and reduced glucagon secretion from the alpha cells. This mechanism helps to lower blood glucose levels in a glucose-dependent manner, thus minimizing the risk of hypoglycemia.

Pharmacodynamics

Teneligliptin exhibits a prolonged duration of action and has a favorable pharmacodynamic profile, leading to improved glycemic control in patients with type 2 diabetes. The increase in incretin hormones contributes to improved beta-cell function and insulin sensitivity. Additionally, teneligliptin may also have beneficial effects on body weight and lipid metabolism, making it a suitable option for overweight patients with type 2 diabetes.

Pharmacokinetics

Teneligliptin is absorbed rapidly following oral administration, with peak plasma concentrations typically reached within a few hours. It has a bioavailability of approximately 60-70%. The drug is extensively metabolized in the liver, primarily via the CYP3A4 pathway, with its elimination occurring mainly through renal excretion. The half-life of teneligliptin is around 10-12 hours, which allows for once-daily dosing. Factors such as renal impairment may necessitate dosage adjustments.

Contra-indications

  • Hypersensitivity to teneligliptin or any of its components
  • Severe renal impairment (eGFR < 15 mL/min)
  • Diabetic ketoacidosis

Adverse effects

  • Hypoglycemia
  • Gastrointestinal disturbances (nausea, vomiting, diarrhea)
  • Headache
  • Dizziness
  • Pancreatitis
  • Allergic reactions (rash, pruritus)

Interactions

  • Caution with concomitant use of medications that affect glycemic control
  • May interact with other antidiabetic agents, which can increase the risk of hypoglycemia
  • Potential interaction with strong CYP3A4 inhibitors and inducers

Precautions

  • Monitor renal function regularly
  • Use with caution in patients with a history of pancreatitis
  • Adjust dose in elderly patients or those with renal impairment

Pregnancy

There is limited data on the use of teneligliptin in pregnancy. It should only be used if the benefits outweigh the risks.

Breast-feeding

It is not known if teneligliptin is excreted in human milk. Caution should be exercised when administered to breastfeeding women.

Storage

Store at room temperature, away from moisture and heat. Keep out of reach of children.

Formulations

  • Tablets of 20 mg

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Molecular reference: teneligliptin

PubChem CID 11949652

Molecular formula: C22H30N6OS

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.