Anpheros Search · Treatment

Repaglinide

Also known as: NovoNorm · Prandin · Repaglinide Teva · Enyglid · Repaglinide Krka

General information only. Anpheros does not diagnose and does not recommend treatment. Talk to a doctor or pharmacist about your situation. In an emergency, call 112 (or your local emergency number).

In short

In the European Union, repaglinide is indicated for patients with type 2 diabetes whose hyperglycaemia can no longer be controlled satisfactorily by diet, weight reduction, and exercise, as well as in combination with metformin when metformin alone is not sufficient. In the United States, repaglinide tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. The medication should not be used in patients with type 1 diabetes mellitus or for the treatment of diabetic ketoacidosis. Repaglinide is listed by the cited source as having an approved use for type 2 diabetes mellitus.

From: Source: European Medicines Agency (EMA), NovoNorm — EPAR, 28/09/2017. © European Medicines Agency. · Data provided by the U.S. Food and Drug Administration. · Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

RxNorm
73044 repaglinide
EMA
EMEA/H/C/000187, EMEA/H/C/000362, EMEA/H/C/001067, EMEA/H/C/001065, EMEA/H/C/001066

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

EMA (EU) NovoNorm

Repaglinide is indicated in patients with type-2 diabetes (non-insulin-dependent diabetes mellitus (NIDDM)) whose hyperglycaemia can no longer be controlled satisfactorily by diet, weight reduction and exercise. Repaglinide is also indicated in combination with metformin in type 2 diabetes patients who are not satisfactorily controlled on metformin alone. Treatment should be initiated as an adjunct to diet and exercise to lower the blood glucose in relation to meals.

Source: European Medicines Agency (EMA), NovoNorm — EPAR, 28/09/2017. © European Medicines Agency.

Document date: 28/09/2017 · Official document →

EMA (EU) Prandin

Repaglinide is indicated in patients with type-2 diabetes (non-insulin-dependent diabetes mellitus (NIDDM)) whose hyperglycaemia can no longer be controlled satisfactorily by diet, weight reduction and exercise. Repaglinide is also indicated in combination with metformin in type-2 diabetes patients who are not satisfactorily controlled on metformin alone. Treatment should be initiated as an adjunct to diet and exercise to lower the blood glucose in relation to meals.

Source: European Medicines Agency (EMA), Prandin — EPAR, 14/05/2018. © European Medicines Agency.

Document date: 14/05/2018 · Official document →

FDA (USA) Repaglinide

1 INDICATIONS AND USAGE Repaglinide tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Limitation of Use: Repaglinide tablets should not be used in patients with type 1 diabetes mellitus or for the treatment of diabetic ketoacidosis. Repaglinide tablets are a glinide indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. (1) Limitation of Use : Not for treatment of type 1 diabetes mellitus or diabetic ketoacidosis (1)

Data provided by the U.S. Food and Drug Administration.

Document date: 20251104 · Official document →

Related terms in the cited sources

Has an official indication for

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External resources

Questions

What is Repaglinide approved for in the European Union?

Repaglinide is indicated in patients with type-2 diabetes (non-insulin-dependent diabetes mellitus (NIDDM)) whose hyperglycaemia can no longer be controlled satisfactorily by diet, weight reduction and exercise. Repaglinide is also indicated in combination with metformin in type 2 diabetes patients who are not satisfactorily controlled on metformin alone. Treatment should be initiated as an adjunct to diet and exercise to lower the blood glucose in relation to meals. (Source: European Medicines Agency (EMA), NovoNorm — EPAR, 28/09/2017. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • Data provided by the U.S. Food and Drug Administration.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), NovoNorm — EPAR, 28/09/2017. © European Medicines Agency.
  • Source: European Medicines Agency (EMA), Prandin — EPAR, 14/05/2018. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →