Glimepiride
Glimepiride is an oral sulfonylurea medication used alongside diet and exercise to help control blood sugar in adults with type 2 diabetes.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 79 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Glimepiride (Amaryl) is a sulfonylurea that lowers blood sugar in adults with type 2 diabetes, alongside diet and exercise, by prompting the pancreas to release more insulin. It is a familiar, low-cost add-on, usually to metformin, on the market since about 1995 and available as a generic. Most people tolerate it well, and what they tend to notice is modest weight gain or an occasional dip in blood sugar. That dip, called hypoglycemia, is the one thing to watch for, with shakiness, sweating, confusion or a racing heart, and it is likeliest after a skipped meal, alcohol or unusual exercise.
Clinical pearls
- Take it with breakfast or your first main meal of the day, because skipping that meal raises the risk of low blood sugar.
- Avoid oral miconazole, an antifungal, because the combination can cause severe low blood sugar.
- Beta-blockers can hide the racing heart of a low, so rely on sweating, shakiness and confusion as your clues instead.
- Older adults and people with kidney disease are more prone to lows, so expect a low starting dose and slow increases.
Patient information guide A plain-language walkthrough of Glimepiride, written from its FDA label.
What Glimepiride is used for
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Glimepiride tablets are used to help control blood sugar in adults with type 2 diabetes. Here is what the FDA-approved product evidence supports:
- Improving blood sugar (glycemic) control in adults with type 2 diabetes, always used together with diet and exercise
- Not approved for type 1 diabetes — it would not be effective
- Not approved for diabetic ketoacidosis (a serious emergency condition)
How Glimepiride works
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Glimepiride is a sulfonylurea. It works by binding to a specific receptor on the insulin-producing beta cells in your pancreas. This binding closes a channel in the cell membrane (called the ATP-sensitive potassium channel), which triggers the cell to release insulin into your bloodstream. That extra insulin helps your body move glucose (sugar) out of the blood and into your cells, lowering your blood sugar level.
Glimepiride dosage
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Glimepiride comes as a tablet taken once daily by mouth. It should always be taken with breakfast or the first main meal of the day to reduce the risk of low blood sugar. Your prescriber will start you on a low dose and increase it gradually — no more often than every one to two weeks — based on your blood sugar readings.
- Take once daily with your first meal
- Do not skip meals after taking your dose
- If you take colesevelam (a cholesterol medicine), take glimepiride at least 4 hours before it
- Follow your prescriber's dosing plan exactly — never adjust your dose on your own
Dosing details from the FDA-approved label
From the Glimepiride prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Recommended dosing (general)
- Starting dose 1 mg or 2 mg once daily, administered with breakfast or the first main meal of the day
- After reaching a daily dose of 2 mg, increase in increments of 1 mg or 2 mg based upon glycemic response
- Uptitration should not occur more frequently than every 1 to 2 weeks
- Maximum: 8 mg once daily
- Administer with breakfast or the first main meal of the day
- Patients at increased risk for hypoglycemia (e.g., the elderly or patients with renal impairment)
- Start on 1 mg once daily
- A conservative titration scheme is recommended
- Maximum: 8 mg once daily
- Elderly or renal impairment: start at 1 mg and titrate slowly
- Patients transferred from longer half-life sulfonylureas (e.g., chlorpropamide)
- May have overlapping drug effect for 1 to 2 weeks and should be appropriately monitored for hypoglycemia
- Monitor for hypoglycemia
- Coadministration with colesevelam
- Administer glimepiride tablets at least 4 hours prior to colesevelam
- Colesevelam reduces glimepiride maximum plasma concentration and total exposure
Read the label’s full dosing text
2 DOSAGE & ADMINISTRATION • Recommended starting dose is 1 or 2 mg once daily. Increase in 1 or 2 mg increments no more frequently than every 1-2 weeks based on glycemic response. Maximum recommended dose is 8 mg once daily. ( 2.1 ) • Administer with breakfast or first meal of the day. ( 2.1 ) • Use 1 mg starting dose and titrate slowly in patients at increased risk for hypoglycemia (e.g., elderly, patients with renal impairment). ( 2.1 ) 2.1 Recommended Dosing • Glimepiride tablets should be administered with breakfast or the first main meal of the day. • The recommended starting dose of glimepiride tablets is 1 mg or 2 mg once daily. Patients at increased risk for hypoglycemia (e.g., the elderly or patients with renal impairment) should be started on 1 mg once daily [ see Warnings and Precautions ( 5.1 ) and Use in Specific Populations ( 8.5 , 8.6 ) ]. After reaching a daily dose of 2 mg, further dose increases can be made in increments of 1 mg or 2 mg based upon the patient's glycemic response. Uptitration should not occur more frequently than every 1 to 2 weeks. A conservative titration scheme is recommended for patients at increased risk for hypoglycemia [ see Warnings and Precautions ( 5.1 ) and Use in Specific Populations ( 8.5 , 8.6 ) ]. • The maximum recommended dose is 8 mg once daily. • Patients being transferred to glimepiride tablets from longer half-life sulfonylureas (e.g., chlorpropamide) may have overlapping drug effect for 1 to 2 weeks and should be appropriately monitored for hypoglycemia. • When colesevelam is coadministered with glimepiride, maximum plasma concentration and total exposure to glimepiride is reduced. Therefore, glimepiride tablets should be administered at least 4 hours prior to colesevelam.
Read the full Dosage and Administration section on DailyMed →
Glimepiride side effects
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The most common side effects reported in clinical trials include:
Common side effects
- Low blood sugar (hypoglycemia) — the most common side effect
- Headache
- Dizziness
- Nausea
- Unintentional weight gain
- Weakness or fatigue
- Skin rash, itching, or redness (less common)
- Elevated liver enzyme levels (seen on blood tests in a small number of patients)
When to get medical help
- Get emergency help right away if you have severe low blood sugar — signs include confusion, seizures, loss of consciousness, or inability to swallow
- Call your doctor immediately if you have signs of a serious allergic reaction: trouble breathing, swelling of the face or throat, severe skin blistering or peeling
- Call your doctor if you notice yellowing of the skin or eyes, dark urine, or severe stomach pain — these may signal liver problems
- Call your doctor if you develop unusual bruising, bleeding, or signs of infection — these could indicate blood cell problems
- Tell your doctor right away if you are pregnant or planning to become pregnant — glimepiride must be stopped at least two weeks before your due date
Glimepiride warnings and precautions
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- Low blood sugar (hypoglycemia): This is the most important risk. It can be severe, cause seizures or loss of consciousness, and may impair driving. Risk is highest in older adults, people with kidney disease, those who skip meals, exercise heavily, or drink alcohol. Some people — especially those on beta-blockers — may not feel the usual warning signs.
- Serious allergic reactions: Rare but potentially life-threatening reactions including anaphylaxis, angioedema (severe swelling), and Stevens-Johnson Syndrome (a severe skin condition) have been reported. Stop glimepiride and seek emergency care if these occur.
- Hemolytic anemia: In people with G6PD deficiency (a genetic enzyme disorder), glimepiride can break down red blood cells. Cases have also been reported in people without known G6PD deficiency.
- Possible cardiovascular risk: Older studies on sulfonylurea-class drugs raised concerns about increased cardiovascular mortality compared to diet alone. Your doctor has considered this when prescribing glimepiride for you.
- No proven cardiovascular benefit: Glimepiride has not been shown in clinical studies to reduce the risk of heart attack, stroke, or other cardiovascular events.
Glimepiride interactions
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Glimepiride can be affected by many common medications and substances. Here are the key ones to know about:
- Oral miconazole (antifungal): Can cause severe low blood sugar — this combination should be avoided
- Other diabetes medications and insulin: Increase the blood-sugar-lowering effect, raising hypoglycemia risk
- Fluconazole (antifungal): Slows the breakdown of glimepiride in the body, raising its levels and increasing low blood sugar risk
- Rifampin (antibiotic): Speeds up glimepiride breakdown, reducing its effectiveness and potentially worsening blood sugar control
- Corticosteroids, diuretics, thyroid hormones, and some other medications: Can weaken glimepiride's effect, leading to higher blood sugar
- Beta-blockers, clonidine, guanethidine, reserpine: Can mask the physical warning signs of low blood sugar (like a fast heartbeat)
- Alcohol: Can unpredictably raise or lower blood sugar — use with caution
- Colesevelam (cholesterol medicine): Reduces glimepiride absorption — always take glimepiride at least 4 hours before colesevelam
Interactions listed in the FDA-approved label
From the Glimepiride prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Drugs that may increase the glucose-lowering effect (e.g., oral anti-diabetic medications, insulin, pramlintide acetate, ACE inhibitors, H2 receptor antagonists, fibrates, fluconazole, clarithromycin, quinolones, tetracyclines, NSAIDs, salicylates, sulfonamides, fluoxetine, coumarins, MAO inhibitors): May increase the glucose-lowering effect of glimepiride, increasing susceptibility to and/or intensity of hypoglycemia. When administered, monitor closely for hypoglycemia; when withdrawn, monitor closely for worsening glycemic control.
- Drugs that may reduce the glucose-lowering effect (e.g., danazol, glucagon, somatropin, protease inhibitors, olanzapine, clozapine, barbiturates, diazoxide, laxatives, rifampin, thiazides and other diuretics, corticosteroids, phenothiazines, thyroid hormones, estrogens, oral contraceptives, phenytoin, nicotinic acid, sympathomimetics, isoniazid): May reduce the glucose-lowering effect of glimepiride, leading to worsening glycemic control. When administered, monitor closely for worsening glycemic control; when withdrawn, monitor closely for hypoglycemia.
- Beta-blockers, clonidine, and reserpine: May lead to either potentiation or weakening of glimepiride's glucose-lowering effect.
- Alcohol: Both acute and chronic alcohol intake may potentiate or weaken the glucose-lowering action of glimepiride in an unpredictable fashion.
- Sympatholytic drugs (beta-blockers, clonidine, guanethidine, reserpine): The signs of hypoglycemia may be reduced or absent.
- Oral miconazole: A potential interaction with sulfonylureas leading to severe hypoglycemia has been reported; whether it occurs with other miconazole dosage forms is not known.
- Fluconazole (cytochrome P450 2C9 inhibitor): May inhibit the metabolism of glimepiride, causing increased plasma concentrations which may lead to hypoglycemia.
- Rifampin (cytochrome P450 2C9 inducer): May induce the metabolism of glimepiride, causing decreased plasma concentrations which may lead to worsening glycemic control.
- Colesevelam: Can reduce the maximum plasma concentration and total exposure of glimepiride when coadministered; absorption is not reduced when glimepiride is given 4 hours prior. Administer glimepiride at least 4 hours prior to colesevelam.
Read the label’s full interactions text
7 DRUG INTERACTIONS • Certain medications may affect glucose metabolism, requiring glimepiride tablets dose adjustment and close monitoring of blood glucose. ( 7.1 ) • Miconazole: Severe hypoglycemia can occur when glimepiride tablets and oral miconazole are used concomitantly. ( 7.2 ) • Cytochrome P450 2C9 interactions: Inhibitors and inducers of cytochrome P450 2C9 may affect glycemic control by altering glimepiride plasma concentrations. ( 7.3 ) • Colesevelam: Coadministration may reduce glimepiride absorption. Glimepiride tablets should be administered at least 4 hours prior to colesevelam. ( 2.1 , 7.4 ) 7.1 Drugs Affecting Glucose Metabolism A number of medications affect glucose metabolism and may require glimepiride dose adjustment and particularly close monitoring for hypoglycemia or worsening glycemic control. The following are examples of medications that may increase the glucose-lowering effect of sulfonylureas including glimepiride, increasing the susceptibility to and/or intensity of hypoglycemia: oral anti-diabetic medications, pramlintide acetate, insulin, angiotensin converting enzyme (ACE) inhibitors, H 2 receptor antagonists, fibrates, propoxyphene, pentoxifylline, somatostatin analogs, anabolic steroids and androgens, cyclophosphamide, phenyramidol, guanethidine, fluconazole, sulfinpyrazone, tetracyclines, clarithromycin, disopyramide, quinolones, and those drugs that are highly protein-bound, such as fluoxetine, nonsteroidal anti-inflammatory drugs, salicylates, sulfonamides, chloramphenicol, coumarins, probenecid and monoamine oxidase inhibitors. When these medications are administered to a patient receiving glimepiride , monitor the patient closely for hypoglycemia. When these medications are withdrawn from a patient receiving glimepiride , monitor the patient closely for worsening glycemic control.
Excerpted — the section continues on the label. Read the full Drug Interactions section on DailyMed →
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Glimepiride
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- Do not take glimepiride if you have ever had an allergic reaction to glimepiride itself, any of its ingredients, or to sulfonamide-type drugs
- Tell your doctor if you have kidney disease — your starting dose will be lower and increases will be made more slowly
- Tell your doctor if you have liver disease — it is not fully known how liver impairment affects glimepiride, so extra caution is needed
- Older adults (65+) are at higher risk for low blood sugar and may need a more conservative dosing approach
- Glimepiride is not recommended for children or teenagers due to effects on body weight and hypoglycemia risk
- If you are pregnant or planning to become pregnant, talk to your doctor right away — glimepiride must be stopped at least two weeks before your expected delivery date to protect the newborn from severe low blood sugar
- If you are breastfeeding, monitor your baby closely for signs of low blood sugar (jitteriness, poor feeding, excessive sleepiness) and discuss the risks and benefits with your doctor
- Tell your doctor if you have G6PD deficiency — a non-sulfonylurea alternative may be safer for you
Glimepiride overdose
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Taking too much glimepiride can cause severe low blood sugar (hypoglycemia). Mild low blood sugar can often be treated by eating or drinking something sugary. Severe cases — especially if the person is confused, having a seizure, or unconscious — are a medical emergency and require immediate treatment with glucagon or intravenous glucose in a hospital setting.
Even after recovery, blood sugar can drop again, so continued monitoring and additional carbohydrate intake may be necessary. If you suspect an overdose, call emergency services right away.
What Glimepiride does in the body
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Glimepiride starts lowering blood sugar after you take it, with its strongest effect occurring roughly 2 to 3 hours after a dose in healthy individuals. It helps lower HbA1c (your average blood sugar over about 3 months), fasting blood sugar, and blood sugar after meals. Like all sulfonylureas, it can also cause modest weight gain over time.
How your body processes Glimepiride
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After taking glimepiride by mouth, blood levels peak in about 2 to 3 hours. Food slightly reduces the peak level but does not meaningfully change overall exposure. The drug is almost entirely bound to proteins in the blood (more than 99.5%) and is completely broken down by the liver — primarily through an enzyme called CYP2C9 — into metabolites that are then cleared mainly through the urine and, to a lesser extent, the stool.
In people with severe kidney disease, breakdown products of glimepiride can build up to much higher levels, increasing the risk of low blood sugar — which is why a lower starting dose is used in those patients. Glimepiride does not meaningfully accumulate in the body with regular daily dosing.
How to store Glimepiride
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Store at 25°C (77°F); excursions permitted to 20°C-25°C (68°F-77°F) . Dispense in well-closed containers with child-resistant closures.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Glimepiride
306 supplements and herbal products have documented interactions with Glimepiride in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 2
- Moderate · 256
- Minor · 48
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
Nutrient depletion considerations
Glimepiride has been associated with lower levels of 1 nutrient in the clinical literature. This does not mean a deficiency will occur — it means these may be worth discussing with your pharmacist or healthcare provider, especially with long-term use.
Educational information from a licensed clinical database (Natural Medicines) — not medical advice. Do not start or stop medications or supplements without professional guidance.
Glimepiride: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Glimepiride — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly is glimepiride supposed to do for me?
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When should I take it, and does it matter if I take it with food?
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What does low blood sugar feel like, and what do I do if it happens?
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Are there any medications or foods I need to be careful about while taking this?
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I'm pregnant — can I keep taking glimepiride?
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Can my child take glimepiride?
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Is Glimepiride available over the counter?
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When was Glimepiride first available?
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Who makes Glimepiride?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Glimepiride on HelloPharmacist
Glimepiride forms and strengths (how it comes)
Glimepiride is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Need a version that does not list lactose, a gluten source, a dye or gelatin? Inactive ingredients differ by manufacturer: see Glimepiride inactive ingredients by manufacturer.
Tablet
How this form is used
- Used to improve blood sugar control in adults with type 2 diabetes, alongside diet and exercise
- Not for treating type 1 diabetes or diabetic ketoacidosis
- Take once daily by mouth with breakfast or your first main meal of the day
- Your prescriber will start you at a low dose and adjust gradually — do not change your dose on your own
- If you also take colesevelam, take glimepiride at least 4 hours before your colesevelam dose
- Patients with kidney problems or older adults should be started at the lowest available dose and increased slowly
Glimepiride on the U.S. market: products, makers and brands
How Glimepiride appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
27 companies list 104 Glimepiride product records with the FDA, mostly as tablet; the earliest marketing or approval year on record is 1995. Brand names on the directory include Amaryl; the rest are generics.
Also listed with the FDA, not a patient dose form: Powder (10) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
How widely Glimepiride is used (Medicaid data)
A general measure of how commonly Glimepiride is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Glimepiride is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Glimepiride prescribed? Of the 1,601 medications we measure, Glimepiride ranks #232 by Medicaid prescriptions — more than 86% of them.
Utilization by Glimepiride product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
glimepiride 4 MG Oral Tablet Most dispensed
Summed across the 15 of 160 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 199247
glimepiride 2 MG Oral Tablet
Summed across the 14 of 157 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 199246
glimepiride 1 MG Oral Tablet
Summed across the 12 of 97 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 199245
glimepiride 3 MG Oral Tablet
Summed across the 1 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 153842
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Glimepiride, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 42 of 417 listed Glimepiride NDCs with Medicaid activity.
Compare Glimepiride products
A representative set of FDA-listed product records for Glimepiride — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Tablet | ||||
| 1 mg | Oral | A-S Medication Solutions × 2 listings | ANDA | View NDC → |
| 2 mg | Oral | A-S Medication Solutions × 6 listings | ANDA | View NDC → |
| 4 mg | Oral | A-S Medication Solutions × 6 listings | ANDA | View NDC → |
| 1 mg | Oral | Accord Healthcare Inc | ANDA | View NDC → |
| 2 mg | Oral | Accord Healthcare Inc | ANDA | View NDC → |
| 4 mg | Oral | Accord Healthcare Inc | ANDA | View NDC → |
| 1 mg | Oral | American Health Packaging | ANDA | View NDC → |
| 2 mg | Oral | American Health Packaging | ANDA | View NDC → |
| 4 mg | Oral | American Health Packaging | ANDA | View NDC → |
| 4 mg | Oral | Aphena Pharma Solutions - Tennessee, LLC | ANDA | View NDC → |
| 1 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 2 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 4 mg | Oral | Aurobindo Pharma Limited | ANDA | View NDC → |
| 1 mg | Oral | AvPAK | ANDA | View NDC → |
| 2 mg | Oral | AvPAK | ANDA | View NDC → |
| 4 mg | Oral | AvPAK | ANDA | View NDC → |
| 1 mg | Oral | BluePoint Laboratories | ANDA | View NDC → |
| 2 mg | Oral | BluePoint Laboratories | ANDA | View NDC → |
| 4 mg | Oral | BluePoint Laboratories | ANDA | View NDC → |
| 1 mg | Oral | Bryant Ranch Prepack × 3 listings | ANDA | View NDC → |
| 2 mg | Oral | Bryant Ranch Prepack × 4 listings | ANDA | View NDC → |
| 4 mg | Oral | Bryant Ranch Prepack × 3 listings | ANDA | View NDC → |
| 2 mg | Oral | Cardinal Health 107, LLC | ANDA | View NDC → |
| 1 mg | Oral | Carlsbad Technology, Inc. | ANDA | View NDC → |
| 2 mg | Oral | Carlsbad Technology, Inc. | ANDA | View NDC → |
| 4 mg | Oral | Carlsbad Technology, Inc. | ANDA | View NDC → |
| 2 mg | Oral | Coupler LLC | ANDA | View NDC → |
| 2 mg | Oral | Direct_Rx | ANDA | View NDC → |
| 4 mg | Oral | Direct_rx | ANDA | View NDC → |
| 1 mg | Oral | Dr. Reddy's Laboratories Limited | ANDA | View NDC → |
| 2 mg | Oral | Dr. Reddy's Laboratories Limited | ANDA | View NDC → |
| 4 mg | Oral | Dr. Reddy's Laboratories Limited | ANDA | View NDC → |
| 1 mg | Oral | Florida Pharmaceutical Products, LLC | ANDA | View NDC → |
| 2 mg | Oral | Florida Pharmaceutical Products, LLC | ANDA | View NDC → |
| 4 mg | Oral | Florida Pharmaceutical Products, LLC | ANDA | View NDC → |
| 1 mg | Oral | Golden State Medical Supply, Inc. | ANDA | View NDC → |
| 2 mg | Oral | Golden State Medical Supply, Inc. | ANDA | View NDC → |
| 4 mg | Oral | Golden State Medical Supply, Inc. | ANDA | View NDC → |
| 3 mg | Oral | Lifsa Drugs LLC | ANDA | View NDC → |
| 1 mg | Oral | Micro Labs Limited | ANDA | View NDC → |
| 2 mg | Oral | Micro Labs Limited | ANDA | View NDC → |
| 3 mg | Oral | Micro Labs Limited | ANDA | View NDC → |
| 4 mg | Oral | Micro Labs Limited | ANDA | View NDC → |
| 6 mg | Oral | Micro Labs Limited | ANDA | View NDC → |
| 8 mg | Oral | Micro Labs Limited | ANDA | View NDC → |
| 1 mg | Oral | NCS HealthCare of KY, Inc dba Vangard Labs | ANDA | View NDC → |
| 2 mg | Oral | NCS HealthCare of KY, Inc dba Vangard Labs | ANDA | View NDC → |
| 4 mg | Oral | NCS HealthCare of KY, Inc dba Vangard Labs | ANDA | View NDC → |
| 2 mg | Oral | Northwind Health Company, LLC × 3 listings | ANDA | View NDC → |
| 4 mg | Oral | Northwind Health Company, LLC × 2 listings | ANDA | View NDC → |
| 2 mg | Oral | NuCare Pharmaceuticals,Inc. × 2 listings | ANDA | View NDC → |
| 4 mg | Oral | NuCare Pharmaceuticals,Inc. | ANDA | View NDC → |
| 1 mg | Oral | PD-Rx Pharmaceuticals, Inc. × 2 listings | ANDA | View NDC → |
| 2 mg | Oral | PD-Rx Pharmaceuticals, Inc. × 4 listings | ANDA | View NDC → |
| 4 mg | Oral | PD-Rx Pharmaceuticals, Inc. × 4 listings | ANDA | View NDC → |
| 2 mg | Oral | Preferred Pharmaceuticals Inc. | ANDA | View NDC → |
| 4 mg | Oral | Preferred Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 1 mg | Oral | Proficient Rx LP × 3 listings | ANDA | View NDC → |
| 2 mg | Oral | Proficient Rx LP × 2 listings | ANDA | View NDC → |
| 4 mg | Oral | Proficient Rx LP × 2 listings | ANDA | View NDC → |
| 2 mg | Oral | Remedyrepack Inc. | ANDA | View NDC → |
| 4 mg | Oral | Remedyrepack Inc. | ANDA | View NDC → |
| 1 mg | Oral | Rising Pharma Holdings, Inc. | ANDA | View NDC → |
| 2 mg | Oral | Rising Pharma Holdings, Inc. | ANDA | View NDC → |
| 4 mg | Oral | Rising Pharma Holdings, Inc. | ANDA | View NDC → |
| 1 mg | Oral | Solco Healthcare U.S., LLC | ANDA | View NDC → |
| 2 mg | Oral | Solco Healthcare U.S., LLC | ANDA | View NDC → |
| 4 mg | Oral | Solco Healthcare U.S., LLC | ANDA | View NDC → |
| 4 mg | Oral | St. Mary's Medical Park Pharmacy × 2 listings | ANDA | View NDC → |
Showing 104 of 104 products — FDA National Drug Code Directory. See every product, package size and price: browse all 104 Glimepiride NDCs →
Glimepiride side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Glimepiride — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Glimepiride in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Glimepiride FDA approval history
How Glimepiride went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Glimepiride recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list 3 Glimepiride recalls since July 2021, covering 7 product listings. Two of them are still ongoing or began in the last six months and are listed first. A recall names specific lots from one company, so check the lot number on your own bottle rather than assuming every product is affected; your pharmacist can check whether your supply came from an affected lot.
- Glimepiride Tablets, USP 1mg, 500-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-05 Lots: Lot: T2303609; Exp. 06/2026 Lot: T2303610; Exp. 06/2026 FDA record D-0313-2024 →
- Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-01 Lots: Lot: T2303622; Exp. 06/2026 Lot: T2303626; Exp. 06/2026 Lot: T2303627; Exp. 06/2026 Lot: T2303628; Exp. 06/2026 Lot: T2303629; Exp. 06/2026 FDA record D-0312-2024 →
- Glimepiride Tablets, USP 4mg, packaged in a) 30-count bottles (NDC 51655-120-52), and b) 90-count bottles (NDC 51655-120-26), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203. Lots: a) Lot #: F105692201, Exp. Date 09/30/2024; F105692203, Exp. Date 02/28/2025 b) Lot #: F105692202, Exp. Date 02/28/2025 FDA record D-0552-2023 →
- Glimepiride Tablets, USP 2mg, packaged in a) 30-count bottles (NDC 51655-383-52), and b)90-count bottles (NDC 51655-383-26), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203. Lots: a) Lot #: F106252201, Exp. Date 09/30/2024; F106252301, F106252303, Exp. Date 5/31/2025; F106252304, Exp. Date 07/31/2025 b) Lot #: F106252302, Exp. Date 07/31/2025 FDA record D-0551-2023 →
- Glimepiride Tablets USP, 4 mg, Rx Only, Packaged in: a) 100-count bottle NDC 16729-003-01 UPC 3 16729 00301 8; b) 500-count NDC 16729-003-16 UPC 3 16729 00316 2; Manufactured for: Accord Healthcare,… Lots: Batches: a) P2001868, Exp. Date 3/31/2023, P2001869 Exp. Date 3/31/2023, P2002810 Exp. Date 5/31/2023, P2005473 Exp. Date 8/31/2023, P2005552 Exp. Date 9/30/2023, P2101986 Exp. Date 3/31/2024, P2101989 Exp. Date 3/31/2024, P2101988 Exp. Da… FDA record D-0395-2023 →
- Glimepiride Tablets USP, 2 mg, Rx Only, Packaged in: a) 100 Tablets NDC 16729-002-01 UPC 3 16729 00201 1; b) 500 Tablets NDC 16729-002-16 UPC 3 16729 00216 5; Manufactured for: Accord Healthcare, Inc… Lots: Batches: a) R2000184, Exp. Date 4/30/2023, R2000183 Exp. Date 4/30/2023, P2002969 Exp. Date 5/31/2023, P2002970 Exp. Date 5/31/2023, P2005346 Exp. Date 8/31/2023, P2005847 Exp. Date 10/31/2023, P2006133 Exp. Date 10/31/2023, P2100682 Exp.… FDA record D-0394-2023 →
- Glimepiride Tablets USP, 1 mg, Rx Only, Packaged in: a) 100-count bottle NDC 16729-001-01 UPC 3 16729 00101 4; b) 500-count bottle NDC 16729-001-16 UPC 3 16729 00116 8; Manufactured for: Accord Healt… Lots: Batches: a) R2000166, Exp. Date 4/30/2023, P2003528 Exp. Date 6/30/2023, P2005451 Exp. Date 8/31/2023, P2005438 Exp. Date 8/31/2023, P2005436 Exp. Date 8/31/2023, P2005437 Exp. Date 8/31/2023, P2005452 Exp. Date 8/31/2023, P2006055 Exp. Da… FDA record D-0393-2023 →
Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 25789 1 dose form · 6 strengths
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Dose form (SCDF) Oral Tablet RxCUI 372319In current FDA listings
Look up RxCUI 25789 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Glimepiride supply and shortage status
Whether Glimepiride is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
Glimepiride brand names
Glimepiride is sold under one brand name in the FDA directory — Amaryl. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Glimepiride: manufacturers and labelers
27 companies list Glimepiride products with the FDA. By number of product records, the largest are A-S Medication Solutions, Bryant Ranch Prepack, PD-Rx Pharmaceuticals, Inc.. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
…and 3 more on the FDA NDC directory.
Sources for this Glimepiride page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. International Laboratories, LLC is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →