Meperidine
Meperidine is a strong opioid pain reliever used for severe pain, as well as before and during surgery and during labor.
🧬 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 2 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 →
⚠️ FDA Boxed Warning — the FDA’s strongest safety alert ▾
Meperidine carries the FDA's most serious warning — a boxed warning — about several life-threatening risks:Breathing can slow or stop. This can happen at any dose, but is most dangerous when starting treatment or increasing the dose. Signs include very slow or shallow breathing or not being able to stay awake.Mixing with other sedatives is extremely dangerous. Combining meperidine with benzodiazepines (like Xanax or Valium), alcohol, or other central nervous system depressants can cause unconsciousness, stopped breathing, and death.MAO inhibitors can cause fatal reactions. Do not take meperidine if you have used an MAO inhibitor in the past 14 days. The combination can cause coma, dangerously low blood pressure, and death.Pregnancy risk: Using meperidine long-term during pregnancy can cause the newborn to go through opioid withdrawal, which can be life-threatening if not treated quickly.Certain drug interactions can cause a fatal overdose — particularly medications that affect CYP3A4 enzymes in the liver. Always tell every provider all the medications you take.
📖 Meperidine: Patient Information Guide
A plain-language walkthrough of Meperidine — 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▾
Meperidine injection is used in specific medical situations where strong opioid pain relief is needed:
- Severe pain that hasn't responded to other treatments
- Preoperative medication — to help patients relax before surgery
- Support of anesthesia during surgical procedures
- Labor and delivery pain (obstetrical analgesia)
⚙️How it works▾
Meperidine is an opioid agonist — it activates opioid receptors in the brain and central nervous system (the brain and spinal cord), much the way morphine does. This activation blocks the perception of pain and produces sedation (calming/drowsiness). It also affects smooth muscle throughout the body, which is why it can cause constipation and other physical effects beyond just pain relief.
💊How it's taken▾
Meperidine is given as an injection — either into muscle or under the skin — by a trained healthcare provider. It is not a self-administered medication at home.
- For pain relief, it is typically given every 3 to 4 hours as needed
- Before surgery, it is given 30 to 90 minutes ahead of time
- During labor, it can be repeated every 1 to 3 hours as needed
Your care team will set the right timing and amount for your individual situation. It is not intended for long-term daily use.
🤒Side effects — in detail▾
The most common side effects with meperidine include:
- Lightheadedness or dizziness
- Drowsiness or sedation
- Nausea and vomiting
- Sweating
- Constipation
- Dry mouth
- Flushing of the face
Serious reactions that need immediate medical attention include stopped or very slow breathing, seizures, severe confusion or hallucinations, and signs of serotonin syndrome such as high fever, agitation, or rapid heart rate. Do not ignore these — get help right away.
⚠️Warnings & precautions▾
- Respiratory depression (breathing slowing or stopping) is the most dangerous risk — it can be life-threatening, especially at the start of treatment or after a dose change.
- Addiction, dependence, and misuse are real risks even when meperidine is used exactly as prescribed. It is a Schedule II controlled substance.
- Normeperidine buildup from extended use can cause tremors, muscle twitching, and seizures — this is why meperidine is not meant for long-term use.
- Mixing with alcohol or sedatives dramatically raises the risk of coma and death.
- Serotonin syndrome — a potentially fatal condition — can occur if meperidine is combined with certain antidepressants or other serotonergic drugs.
- Head injury or high intracranial pressure (pressure inside the skull): meperidine can worsen these conditions and should be used very carefully or avoided.
- Neonatal opioid withdrawal syndrome: babies born to mothers who used meperidine long-term may experience serious withdrawal symptoms at birth.
🔀What it interacts with▾
Meperidine interacts with several medications — some combinations are outright dangerous:
- MAO inhibitors (phenelzine, tranylcypromine, linezolid) — absolutely contraindicated; can cause coma, dangerously low blood pressure, and death; must be stopped at least 14 days before using meperidine
- Benzodiazepines and CNS depressants (Xanax, Valium, sleep aids) — dangerous sedation and breathing suppression
- Alcohol — adds to sedation and raises risk of breathing problems
- CYP3A4 inhibitors (certain antifungals, some antibiotics, HIV medications like ritonavir) — raise meperidine blood levels, increasing overdose risk
- CYP3A4 inducers (like phenytoin) — change the way meperidine breaks down and may raise levels of normeperidine, the toxic byproduct
- Serotonergic drugs (certain antidepressants, triptans for migraines) — risk of serotonin syndrome
- Acyclovir and cimetidine — can increase meperidine or normeperidine levels in the blood
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▾
- Taking MAO inhibitors or took them in the last 14 days — this combination is contraindicated (not allowed)
- Significant breathing problems or severe asthma — meperidine can worsen respiratory depression
- Known allergy or hypersensitivity to meperidine
- Bowel obstruction or paralytic ileus (blocked intestines) — contraindicated
- History of substance use disorder or addiction — risk is higher
- Pregnant women — long-term use can harm the fetus and cause newborn withdrawal; use during labor may cause breathing problems in the newborn
- Older adults — meperidine stays in the body longer; start cautiously and monitor closely
- Liver or kidney impairment — meperidine and its byproduct are cleared more slowly, raising the risk of buildup and toxicity
- Head injury, brain tumor, or increased intracranial pressure — meperidine can mask symptoms and worsen these conditions
- Circulatory shock or very low blood pressure — meperidine should be avoided in these situations
🚑If you take too much▾
Too much meperidine can cause breathing to slow dramatically or stop, extreme sleepiness progressing to unconsciousness, limpness, pinpoint (very small) pupils, cold clammy skin, and in severe cases, cardiac arrest and death. Buildup of normeperidine — the breakdown product — can cause the opposite: agitation, tremors, muscle twitching, enlarged pupils, and seizures.
If overdose is suspected, call 911 immediately. A reversal agent called naloxone can counteract meperidine's effects, but medical monitoring is still needed because meperidine may last longer than the reversal agent.
📡Pharmacodynamics — effects in the body▾
Meperidine slows breathing by directly suppressing the brain centers that control it. It causes the pupils to constrict (become very small) — pinpoint pupils are a known sign of opioid overdose. It also slows movement through the digestive tract, which leads to constipation and can cause spasms in the bile ducts. On the cardiovascular side, it widens blood vessels (vasodilation), which can cause blood pressure to drop, especially when standing up quickly. With extended use, it can disrupt hormonal systems, potentially affecting sex hormones and leading to issues such as low sex drive or irregular periods.
🔬Pharmacokinetics — how your body processes it▾
Meperidine is broken down (metabolized) mainly in the liver by enzymes called CYP3A4 and CYP2B6 into a byproduct called normeperidine. Meperidine itself clears from the body in about 3 to 8 hours in healthy people, but normeperidine lingers much longer — around 20 hours on average — which is why it can accumulate with repeated dosing. Both meperidine and normeperidine are cleared through the kidneys. In people with liver disease or in older adults, meperidine is processed more slowly, meaning the drug and its byproduct stay in the body longer and are more likely to build up to harmful levels. Certain other medications (like ritonavir, acyclovir, or phenytoin) can also significantly change how meperidine is processed.
📦How to store it▾
Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C to 30°C (59°F to 86°F).
📄 Written from Meperidine’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 →
Supplements & herbs that interact with Meperidine
155 supplements and herbal products have documented interactions with Meperidine in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 8
- Moderate · 124
- Minor · 23
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.
🩺 Pharmacist Counseling Corner
Quick, plain-English answers to the questions patients ask most about Meperidine — the kind of thing our pharmacy team would talk through with you at the counter.
Why was I given meperidine instead of another pain medication? ▾
Is it safe to drink alcohol while receiving meperidine? ▾
What side effects should I just expect, versus what should I call for help about? ▾
Can I take meperidine if I'm also on an antidepressant? ▾
I'm pregnant — is meperidine safe for my baby? ▾
Why did I hear that meperidine isn't supposed to be used for a long time? ▾
Is Meperidine available over the counter? ▾
Is Meperidine a controlled substance? ▾
When was Meperidine first available? ▾
Who makes Meperidine? ▾
💬 Answers drafted from Meperidine’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 Meperidine comes
Meperidine is available in 3 forms. 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.
📊 Meperidine across the U.S. market
How Meperidine 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.
FDA-listed product records by dose form (tablet variants merged) — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
Also listed with the FDA, not a patient dose form: Powder (7) — 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 Meperidine is used
A general measure of how commonly Meperidine 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 Meperidine 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 Meperidine prescribed? Of the 1,596 medications we measure, Meperidine ranks #939 by Medicaid prescriptions — more than 41% of them.
Utilization by Meperidine 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.
meperidine hydrochloride 10 MG/ML Oral Solution Most dispensed
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 861479
1 ML meperidine hydrochloride 25 MG/ML Injection
Summed across the 1 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 861476
1 ML meperidine hydrochloride 25 MG/ML Cartridge
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 861494
1 ML meperidine hydrochloride 50 MG/ML Injection
Summed across the 1 of 3 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1665697
1 ML meperidine hydrochloride 100 MG/ML Injection
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1665685
1 ML meperidine hydrochloride 50 MG/ML Cartridge
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 861473
1 ML meperidine hydrochloride 100 MG/ML Cartridge
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 861493
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 Meperidine, 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 7 of 15 listed Meperidine NDCs with Medicaid activity.
🔍 Compare Meperidine products
A representative set of FDA-listed product records for Meperidine — 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 | ||||
| 25 mg/mL | Intramuscular, Intravenous, Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 25 mg/mL | Intramuscular; Intravenous; Subcutaneous | Hikma Pharmaceuticals USA Inc. × 2 listings | ANDA | View NDC → |
| 50 mg/mL | Intramuscular, Intravenous, Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 50 mg/mL | Intramuscular; Intravenous; Subcutaneous | Hikma Pharmaceuticals USA Inc. × 2 listings | ANDA | View NDC → |
| 100 mg/mL | Intramuscular, Intravenous, Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 100 mg/mL | Intramuscular; Intravenous; Subcutaneous | Hikma Pharmaceuticals USA Inc. × 2 listings | ANDA | View NDC → |
| 25 mg/mL | Intramuscular, Intravenous, Subcutaneous | Hospira, Inc. × 2 listings | NDA | View NDC → |
| 25 mg/mL | Intramuscular; Intravenous; Subcutaneous | Hospira, Inc. × 4 listings | NDA | View NDC → |
| 50 mg/mL | Intramuscular, Intravenous, Subcutaneous | Hospira, Inc. × 4 listings | NDA | View NDC → |
| 50 mg/mL | Intramuscular; Intravenous; Subcutaneous | Hospira, Inc. × 6 listings | NDA | View NDC → |
| 75 mg/mL | Intramuscular, Intravenous, Subcutaneous | Hospira, Inc. | NDA | View NDC → |
| 75 mg/mL | Intramuscular; Intravenous; Subcutaneous | Hospira, Inc. × 2 listings | NDA | View NDC → |
| 100 mg/mL | Intramuscular; Intravenous; Subcutaneous | Hospira, Inc. × 2 listings | NDA | View NDC → |
| 💊Oral solution | ||||
| 50 mg/5 mL | Oral | Hikma Pharmaceuticals USA Inc. × 2 listings | ANDA | View NDC → |
| 50 mg/5 mL | Oral | West-Ward Pharmaceuticals Corp. | ANDA | View NDC → |
| 💊Tablet | ||||
| 50 mg | Oral | Epic Pharma, Llc × 3 listings | ANDA | View NDC → |
| 100 mg | Oral | Epic Pharma, Llc × 3 listings | ANDA | View NDC → |
| 50 mg | Oral | Genus Lifesciences Inc. | ANDA | View NDC → |
| 50 mg | Oral | Validus Pharmaceuticals LLC × 2 listings | NDA | View NDC → |
| 100 mg | Oral | Validus Pharmaceuticals LLC × 2 listings | NDA | View NDC → |
| 💊Bulk drug substance | ||||
| 20 kg/20 kg | — | Curia New York, Inc. × 2 listings | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING | View NDC → |
| 1 g/g | — | Medisca Inc. | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Pharma Source Direct, Inc. | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING | View NDC → |
| 1 kg/kg | — | Professional Compounding Centers of America dba PCCA | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING | View NDC → |
| 1 kg/kg | — | SpecGx LLC | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Spectrum Laboratory Products, Inc. | BULK INGREDIENT | View NDC → |
Showing 51 of 51 products — FDA National Drug Code Directory. See every product, package size and price: browse all 51 Meperidine 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 Meperidine — 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 Meperidine 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 Meperidine 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 6754 6 dose forms · 16 strengths
-
Dose form (SCDF) Cartridge RxCUI 1665009No current FDA listingClinical drug / strength (SCD) 1 ML meperidine hydrochloride 100 MG/MLRxCUI 8614931 ML meperidine hydrochloride 25 MG/MLRxCUI 8614941 ML meperidine hydrochloride 50 MG/MLRxCUI 8614731 ML meperidine hydrochloride 75 MG/MLRxCUI 860792 -
Dose form (SCDF) Injectable Solution RxCUI 372764In current FDA listingsClinical drug / strength (SCD) hydrochloride 10 MG/MLRxCUI 861447hydrochloride 100 MG/MLRxCUI 861459hydrochloride 50 MG/MLRxCUI 861463 -
Dose form (SCDF) Injection RxCUI 1665037In current FDA listingsClinical drug / strength (SCD) 1 ML meperidine hydrochloride 100 MG/MLRxCUI 16656851 ML meperidine hydrochloride 25 MG/MLRxCUI 8614761 ML meperidine hydrochloride 50 MG/MLRxCUI 16656971 ML meperidine hydrochloride 75 MG/MLRxCUI 861482 -
Dose form (SCDF) Oral Solution RxCUI 608008In current FDA listingsClinical drug / strength (SCD) hydrochloride 10 MG/MLRxCUI 861479 -
Dose form (SCDF) Oral Tablet RxCUI 372766In current FDA listings -
Dose form (SCDF) Prefilled Syringe RxCUI 727616No current FDA listingClinical drug / strength (SCD) 1 ML meperidine hydrochloride 25 MG/MLRxCUI 25391911 ML meperidine hydrochloride 50 MG/MLRxCUI 2539186
Look up RxCUI 6754 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 Meperidine 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
Meperidine belongs to the Opioid Agonist 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 2 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. Hospira, Inc. 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.