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Glimepiride 2 mg Tablet

NAFDAC Reg. No. A4-101238 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Glimepiride 2 mg Tablet
NAFDAC number
A4-101238
Active ingredient
Glimepiride
Strength
2 mg
Form
Tablet
Pack size
3 × 10's (in Alu-PVDC blisters)
Manufacturer
Not listed
Applicant (holder)
Swiss Pharma Nigeria Limited
Approved
30 Apr 2025
Status
Active View on NAFDAC ↗
Registration valid to
29 Apr 2030
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Glimepiride 2 mg Tablet is on the NAFDAC register with an active registration (A4-101238). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

What Glimepiride 2 mg Tablet is used for

From the official U.S. FDA label for glimepiride, the active ingredient registered with NAFDAC.

What it is used for

Glimepiride tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus [see Clinical Studies (14.1) ]. Limitations of Use Glimepiride tablets should not be used for the treatment of type 1 diabetes mellitus or diabetic ketoacidosis, as it would not be effective in these settings. Glimepiride tablets are a sulfonylurea indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus ( 1 ). Limitations of Use: Not for treating type 1 diabetes mellitus or diabetic ketoacidosis ( 1 ).

Possible side effects

The following serious adverse reactions are discussed in more detail below and elsewhere in the labeling: Hypoglycemia [see Warnings and Precautions (5.1) ] Hemolytic anemia [see Warnings and Precautions (5.3) ] In clinical trials, the most common adverse reactions with glimepiride were hypoglycemia, dizziness, asthenia, headache, and nausea. Common adverse reactions in clinical trials (≥5% and more common than with placebo) include hypoglycemia, headache, nausea, and dizziness ( 6.1 ). To report SUSPECTED ADVERSE REACTIONS, contact Dr. Reddy’s Laboratories, Inc. at 1-888-375-3784 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . …

Do not use if

Glimepiride tablets are contraindicated in patients with a history of a hypersensitivity reaction to: Glimepiride or any of the product’s ingredients [see Warnings and Precautions (5.2) ]. Sulfonamide derivatives: Patients who have developed an allergic reaction to sulfonamide derivatives may develop an allergic reaction to glimepiride. Do not use glimepiride in patients who have a history of an allergic reaction to sulfonamide derivatives. …

Warnings

Hypoglycemia: May be severe. Ensure proper patient selection, dosing, and instructions, particularly in at-risk populations (e.g., elderly, renally impaired) and when used with other anti-diabetic medications ( 5.1 ). Hypersensitivity Reactions: Postmarketing reports include anaphylaxis, angioedema and Stevens-Johnson Syndrome. If a reaction is suspected, promptly discontinue glimepiride, assess for other potential causes for the reaction, and institute alternative treatment for diabetes ( 5.2 ). Hemolytic Anemia: Can occur if glucose 6-phosphate dehydrogenase (G6PD) deficient. Consider a non-sulfonylurea alternative. ( 5.3 ). …

Pregnancy & breastfeeding

8.1 Pregnancy Risk Summary Available data from a small number of published studies and postmarketing experience with glimepiride use in pregnancy over decades have not identified any drug associated risks for major birth defects, miscarriage, or adverse maternal outcomes. However, sulfonylureas (including glimepiride) cross the placenta and have been associated with neonatal adverse reactions such as hypoglycemia. …

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Glimepiride 2 mg Tablet

Add the expiry date on your pack for a full Trust Score.

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Glimepiride 2 mg Tablet

What is in Glimepiride 2 mg Tablet?

Glimepiride 2 mg Tablet contains Glimepiride (2 mg), as tablet, according to its NAFDAC registration record.

Is Glimepiride 2 mg Tablet registered with NAFDAC?

Yes. Glimepiride 2 mg Tablet is listed on the NAFDAC register under registration number A4-101238, and its registration is active as of 28 October 2026.

Has Glimepiride 2 mg Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Glimepiride 2 mg Tablet in our automatically synced alert list.

How can I check that my pack of Glimepiride 2 mg Tablet is genuine?

Run a free authenticity scan with the NAFDAC number A4-101238, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Glimepiride 2 mg Tablet used for?

Glimepiride tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus [see Clinical Studies (14.1) ]. Limitations of Use Glimepiride tablets should not be used for the treatment of type 1 diabetes mellitus or diabetic ketoacidosis, as it would not be effective in these settings. Glimepiride tablets are a sulfonylurea indicated as a (Summarised from the official U.S. FDA label for glimepiride. Always follow your doctor or pharmacist.)

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