Meropenem
Meropenem is a broad-spectrum intravenous antibiotic used to treat serious bacterial infections including complicated skin and skin structure infections, complicated intra-abdominal infections, and bacterial meningitis.
🧬 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 23 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 →
📖 Meropenem: Patient Information Guide
A plain-language walkthrough of Meropenem — what it treats, how it works, how it’s taken, side effects, warnings and interactions. Tap any section to expand it.
🎯What it's used for▾
Meropenem for injection is a broad-spectrum IV antibiotic approved for several serious bacterial infections across different patient populations.
- Complicated skin and skin structure infections: Approved for adults and pediatric patients 3 months of age and older — caused by specific bacteria including Staphylococcus aureus (methicillin-susceptible strains only), Pseudomonas aeruginosa, E. coli, and others
- Complicated intra-abdominal infections (including complicated appendicitis and peritonitis): Approved for adults and pediatric patients of all ages, including infants less than 3 months old
- Bacterial meningitis: Approved for pediatric patients 3 months of age and older only — caused by Haemophilus influenzae, Neisseria meningitidis, and penicillin-susceptible Streptococcus pneumoniae
⚙️How it works▾
Meropenem is a carbapenem antibiotic that kills bacteria by blocking their ability to build and maintain their outer cell wall. Bacteria need an intact cell wall to survive — without it, they break down and die. Because meropenem works against a wide variety of both gram-positive and gram-negative bacteria, it's reserved for serious infections where broad coverage is needed.
How well meropenem works is closely tied to how long its concentration in the blood stays above the minimum level needed to inhibit the target bacteria. This is why dosing intervals and infusion timing matter clinically.
💊How it's taken▾
Meropenem is given only by intravenous (IV) infusion or bolus injection — never by mouth. It is typically administered every 8 hours, though the exact interval and amount depend on the type of infection, the patient's age, and kidney function. Adults with reduced kidney function (creatinine clearance of 50 mL/min or less) require dose adjustments. In young infants, dosing intervals are based on gestational age and postnatal age.
- IV infusions are generally given over 15 to 30 minutes; certain doses may also be given as a short bolus over 3 to 5 minutes
- For infants under 3 months, infusions are given over 30 minutes
- Because this is a hospital IV medication, a healthcare provider manages each dose — follow the schedule your care team sets
🤒Side effects — in detail▾
The most commonly reported side effects with meropenem include:
- Diarrhea
- Nausea and vomiting
- Headache
- Rash or itching
- Constipation
- Injection site reactions — redness, pain, or inflammation where the IV is placed
- Anemia (low red blood cell count)
Serious reactions to watch for include severe allergic reactions (difficulty breathing, swelling, hives), blistering or peeling skin rashes, muscle breakdown (rhabdomyolysis), seizures, and severe or persistent diarrhea that could signal a C. difficile infection. Get medical help right away if any of these occur.
⚠️Warnings & precautions▾
- Severe allergic reactions: Life-threatening anaphylaxis has occurred with this class of drugs. People with penicillin or other beta-lactam allergies are at higher risk. Meropenem must be stopped immediately if an allergic reaction occurs.
- Serious skin reactions: Rare but potentially fatal skin conditions — including Stevens-Johnson syndrome and toxic epidermal necrolysis — have been reported. Stop meropenem immediately if blistering or severe rash appears.
- Seizure risk: Seizures are more likely in patients with brain conditions, a history of seizures, or kidney impairment. Patients already on anti-seizure medications should continue them during treatment.
- Valproic acid interaction: Meropenem can dramatically lower blood levels of valproic acid (used for seizures), potentially causing breakthrough seizures. This combination is generally not recommended.
- C. difficile-associated diarrhea: Like all antibiotics, meropenem can disrupt gut bacteria and allow C. difficile to overgrow, causing diarrhea that can range from mild to life-threatening colitis.
- Rhabdomyolysis: Rare reports of muscle breakdown — watch for muscle pain, weakness, or dark urine and report immediately.
- Thrombocytopenia: Low platelet counts have been observed in patients with kidney impairment.
🔀What it interacts with▾
Meropenem has two clinically important drug interactions identified in the label:
- Probenecid (used for gout or certain kidney conditions): Blocks the kidneys from clearing meropenem normally, raising meropenem levels in the blood. Co-administration is not recommended.
- Valproic acid or divalproex sodium (seizure medications): Meropenem significantly reduces blood levels of these drugs, which can cause previously controlled seizures to return. Alternative antibiotics should be used when possible. If meropenem is necessary, additional seizure precautions should be taken.
This is not a complete list of interactions. Always talk with your doctor or pharmacist before starting, stopping, or changing any medication.
📋Before taking it▾
- Tell your doctor if you have ever had a severe allergic reaction — especially to penicillin, cephalosporins, or any other antibiotic — before starting meropenem
- Tell your doctor about any history of seizures or brain conditions — meropenem can increase seizure risk in these patients
- Tell your doctor if you take valproic acid or divalproex sodium for seizures — meropenem can dangerously lower those drug levels
- Tell your doctor if you have kidney disease — the dose must be reduced when kidney function is impaired
- Older adults are more likely to have reduced kidney function and may need dose adjustments and closer monitoring
- If you are pregnant, the risks are not fully known in humans — discuss the benefits and risks with your doctor
- Meropenem passes into breast milk — talk with your doctor about the risks to a nursing infant before breastfeeding
- Meropenem is established as safe and effective in children 3 months and older for skin and meningitis uses, and in children of all ages for intra-abdominal infections
🚑If you take too much▾
An accidental overdose is most likely to happen in patients with poor kidney function who receive too large a dose. In such cases, any side effects that occur are generally consistent with the known side effect profile and tend to be mild. Meropenem and its breakdown product can be removed from the body by hemodialysis (dialysis), though dialysis specifically to treat overdose has not been studied.
📡Pharmacodynamics — effects in the body▾
Meropenem's effectiveness is most closely tied to how long its concentration in the blood stays above the minimum level needed to stop the target bacteria from growing — a concept called time-dependent killing. Maintaining adequate drug exposure throughout each dosing interval is key to the antibiotic working properly. This is why careful attention to dosing frequency and infusion timing is important in clinical practice.
🔬Pharmacokinetics — how your body processes it▾
After an IV dose, meropenem spreads quickly and widely into body tissues and fluids — including the lungs, skin, peritoneal fluid, and, in inflamed meninges, the cerebrospinal fluid (fluid around the brain and spinal cord). It binds very little to proteins in the blood (about 2%), meaning most of the drug is free and active. Meropenem has a short half-life of about 1 hour in adults with normal kidney function, so it clears the body relatively quickly. About 70% of the dose is excreted unchanged through the kidneys within 12 hours, making kidney function a critical factor in dosing — people with reduced kidney function clear the drug more slowly and need lower or less frequent doses.
📦How to store it▾
stored at 20°–25°C (68°–77°F) .
📄 Written from Meropenem’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Every point is grounded in that labeling — nothing is invented. How we use AI →
🩺 Pharmacist Counseling Corner
Quick, plain-English answers to the questions patients ask most about Meropenem — the kind of thing our pharmacy team would talk through with you at the counter.
Why am I getting meropenem instead of a regular antibiotic pill? ▾
What side effects should I actually watch out for? ▾
I take valproic acid for my seizures — is that a problem with meropenem? ▾
I'm allergic to penicillin — is it safe for me to get meropenem? ▾
My kidneys aren't working great — does that affect how I get this medication? ▾
Can I breastfeed while receiving meropenem? ▾
Is Meropenem available over the counter? ▾
When was Meropenem first available? ▾
Who makes Meropenem? ▾
💬 Answers drafted from Meropenem’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Grounded in that labeling — nothing is made up. How we use AI →
🧰 Keep exploring
💊 How Meropenem comes
Meropenem 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.
Injection
How this form is used
- Treats complicated skin and skin structure infections in adults and children 3 months of age and older
- Treats complicated intra-abdominal infections (including appendicitis and peritonitis) in adults and children of all ages
- Treats bacterial meningitis in children 3 months of age and older
- Given by intravenous (IV) infusion over approximately 15 to 30 minutes, or as an IV bolus injection over 3 to 5 minutes, depending on the dose and indication
- Typically administered every 8 hours, though frequency may change based on infection type and kidney function
- Dose must be reduced in adult patients with reduced kidney function (creatinine clearance 50 mL/min or less)
- For infants less than 3 months of age with intra-abdominal infections, the IV infusion is given over 30 minutes; dosing interval varies by gestational and postnatal age
Show 1 more strength Show fewer strengths
📊 Meropenem across the U.S. market
How Meropenem 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.
Also listed with the FDA, not a patient dose form: Powder (3) — 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 Meropenem is used
A general measure of how commonly Meropenem 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 Meropenem 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 Meropenem prescribed? Of the 1,596 medications we measure, Meropenem ranks #733 by Medicaid prescriptions — more than 54% of them.
Utilization by Meropenem 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.
meropenem 1000 MG Injection Most dispensed
Summed across the 15 of 43 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1722939
meropenem 500 MG Injection
Summed across the 12 of 43 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1722934
meropenem 2000 MG Injection
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2664894
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 Meropenem, 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 29 of 92 listed Meropenem NDCs with Medicaid activity.
🔍 Compare Meropenem products
A representative set of FDA-listed product records for Meropenem — 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 |
|---|---|---|---|---|
| 💊Injection | ||||
| 500 mg/20 mL | Intravenous | Amneal Pharmaceuticals LLC × 3 listings | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Amneal Pharmaceuticals LLC × 3 listings | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Armas Pharmaceuticals Inc × 2 listings | ANDA | View NDC → |
| 1 g/20 mL | Intravenous | Armas Pharmaceuticals Inc × 2 listings | ANDA | View NDC → |
| 500 mg | Intravenous | AuroMedics Pharma LLC | ANDA | View NDC → |
| 1 g | Intravenous | AuroMedics Pharma LLC | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | BluePoint Laboratories × 3 listings | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | BluePoint Laboratories × 3 listings | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Brooks Steriscience Limited × 3 listings | ANDA | View NDC → |
| 1 g/20 mL | Intravenous | Brooks Steriscience Limited × 3 listings | ANDA | View NDC → |
| 2 g | Intravenous | Brooks Steriscience Limited | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Civica, Inc × 3 listings | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Civica, Inc × 3 listings | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Civica, Inc. | ANDA | View NDC → |
| 1 g/20 mL | Intravenous | Civica, Inc. | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Daewoong America Inc. | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Daewoong America Inc. | ANDA | View NDC → |
| 500 mg | Intravenous | Eugia US LLC × 2 listings | ANDA | View NDC → |
| 1 g | Intravenous | Eugia US LLC × 2 listings | ANDA | View NDC → |
| 500 mg/10 mL | Intravenous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 1 g/20 mL | Intravenous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Gland Pharma Limited × 2 listings | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Gland Pharma Limited × 2 listings | ANDA | View NDC → |
| 500 mg/10 mL | Intravenous | Hikma Pharmaceuticals USA Inc. × 2 listings | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 1 g/20 mL | Intravenous | Hikma Pharmaceuticals USA Inc. × 2 listings | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 500 mg/10 mL | Intravenous | Hospira, Inc. × 5 listings | ANDA | View NDC → |
| 1 g/20 mL | Intravenous | Hospira, Inc. × 5 listings | ANDA | View NDC → |
| 2 g | Intravenous | Mylan Institutional LLC | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Pfizer Laboratories Div Pfizer Inc | NDA | View NDC → |
| 500 mg/20 mL | Intravenous | Qilu Antibiotics Pharmaceutical Co., Ltd. | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Qilu Antibiotics Pharmaceutical Co., Ltd. | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Sagent Pharmaceuticals | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Sagent Pharmaceuticals | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Sandoz Inc × 3 listings | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Sandoz Inc × 3 listings | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Savior Lifetec Corporation × 2 listings | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Savior Lifetec Corporation × 2 listings | ANDA | View NDC → |
| 500 mg | Intravenous | WG Critical Care, LLC × 6 listings | ANDA | View NDC → |
| 1 g | Intravenous | WG Critical Care, LLC × 6 listings | ANDA | View NDC → |
| 2 g | Intravenous | WG Critical Care, LLC × 4 listings | NDA | View NDC → |
| 500 mg | Intravenous | Xellia Pharmaceuticals USA LLC | ANDA | View NDC → |
| 500 mg/20 mL | Intravenous | Xellia Pharmaceuticals USA LLC × 2 listings | ANDA | View NDC → |
| 1 g | Intravenous | Xellia Pharmaceuticals USA LLC | ANDA | View NDC → |
| 1 g/30 mL | Intravenous | Xellia Pharmaceuticals USA LLC × 2 listings | ANDA | View NDC → |
| 💊Bulk drug substance | ||||
| 1 kg/kg | — | ACS Dobfar S.p.A | BULK INGREDIENT | View NDC → |
| 5 kg/5.9 kg | — | Sumitomo Pharma Co., Ltd. | DRUG FOR FURTHER PROCESSING | View NDC → |
| 12 kg/12 kg | — | Sumitomo Pharma Co., Ltd. | BULK INGREDIENT | View NDC → |
Showing 106 of 106 products — FDA National Drug Code Directory. See every product, package size and price: browse all 106 Meropenem NDCs →
📈 What people report — real-world data (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 Meropenem — 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 Meropenem 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.
🏛️ The road to your pharmacy
How Meropenem went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
🚨 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.
Source: openFDA drug enforcement (recall) reports.
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 29561 1 dose form · 3 strengths
-
Dose form (SCDF) Injection RxCUI 1722933In current FDA listings
Look up RxCUI 29561 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.
📦 Supply & shortage status
Whether Meropenem 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.
🏷️ Sold under these brand names
🏭 Manufacturers & labelers
RxNorm drug class
Meropenem belongs to the Penem Antibacterial class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
🔬 Where this comes from
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 we combine label and product data
HelloPharmacist combines public FDA and NLM records; we don’t author the underlying clinical facts. We identified 23 FDA-filed SPL label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. The representative label is the starting point for the displayed reference monograph; the 12 largest stored in-scope SPL records, which may include that representative, are compared section by section, and the longest available version of each section is retained. Forms, routes, brands, labelers, product-listed strengths, and product-record counts are aggregated separately from ingredient-matched FDA NDC Directory records; package records listed above are associated with the linked SPL; and the normalized concept hierarchy comes from NLM RxNorm.
For canonical ingredient pages, bounded product-attributed indication and administration excerpts may be added to the AI evidence, and the generator is instructed to preserve available product, brand, route, and form qualifiers instead of treating one label as universal. Where a section is identified as AI-written, its plain-language text is generated from bounded label evidence. New draft drug pages remain in the admin review queue before first publication. WG Critical Care, LLC is the representative DailyMed label linked for verification and dates; it is not the sole source used for the page.
This is general education, not medical advice — always consult your doctor or pharmacist about your medications and any medical condition. For the exact wording of the linked representative label, view that label on DailyMed; some displayed composite sections may come from other in-scope SPL labels. Learn how we use AI and our data sources & update cadence.