Enoxaparin
Enoxaparin is a blood thinner (anticoagulant) used to prevent and treat dangerous blood clots, including deep vein thrombosis, pulmonary embolism, and clot-related complications of unstable angina and heart attack.
🧬 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 30 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 ▾
Serious warning: Enoxaparin can cause dangerous bleeding inside the spine. If you receive enoxaparin while also getting spinal or epidural anesthesia, or having a spinal puncture (spinal tap), there is a risk of bleeding into the space around your spinal cord — called a spinal or epidural hematoma. This can press on your spinal cord and cause long-term or permanent paralysis.
Your risk is higher if you have an indwelling epidural catheter (a tube left in your spine for pain control), take other drugs that affect bleeding (like NSAIDs, aspirin, or other blood thinners), have had multiple or difficult spinal procedures in the past, or have a history of spinal surgery or a spinal deformity. Watch for new numbness or weakness in your legs, loss of bladder or bowel control, or back pain — and get emergency medical help immediately if any of these occur.
📖 Enoxaparin: Patient Information Guide
A plain-language walkthrough of Enoxaparin — 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▾
Enoxaparin is a low molecular weight heparin (LMWH) approved for several blood clot-related conditions across multiple products and formulations.
- Prevention of deep vein thrombosis (DVT): For patients having abdominal surgery, hip replacement surgery, or knee replacement surgery who are at risk for clots; also for hospitalized medical patients whose movement is severely restricted during acute illness
- Treatment of acute DVT with pulmonary embolism (inpatient): Enoxaparin Sodium Injection and Lovenox are used alongside warfarin for inpatient DVT treatment, with or without a pulmonary embolism
- Treatment of acute DVT without pulmonary embolism (outpatient): Enoxaparin Sodium Injection and Lovenox are used alongside warfarin for outpatient DVT treatment when there is no pulmonary embolism
- Prevention of ischemic complications of unstable angina and non-Q-wave myocardial infarction: Enoxaparin Sodium Injection and Lovenox are given with aspirin to reduce the risk of dangerous tissue damage from reduced blood flow in these cardiac conditions
- Treatment of acute STEMI (ST-segment elevation myocardial infarction): Enoxaparin Sodium Injection and Lovenox are used for STEMI managed medically or with percutaneous coronary intervention (PCI)
⚙️How it works▾
Enoxaparin works by blocking clotting proteins in the blood — most importantly a protein called Factor Xa — which disrupts the clotting cascade and prevents dangerous blood clots from forming or getting larger. Compared to regular heparin, enoxaparin has a much stronger effect on Factor Xa relative to its effect on thrombin (another clotting protein), which gives it a more predictable, targeted anticoagulant effect.
💊How it's taken▾
Enoxaparin is given as an injection — most commonly under the skin (subcutaneously) — once or twice a day, depending on what it's being used for. In certain heart attack situations, an initial dose may be given directly into a vein (intravenously) followed by subcutaneous injections. It can be given regardless of meals since it's injected, not swallowed.
- Timing of doses around surgery, spinal procedures, or epidural catheters is especially important — your medical team will set this carefully
- Never skip or double up on doses without guidance from your prescriber
- Follow your prescriber's and pharmacist's instructions exactly for your specific condition and product
🤒Side effects — in detail▾
The most common side effects of enoxaparin relate to its blood-thinning action:
- Bleeding (can range from minor bruising to serious internal bleeding)
- Anemia (low red blood cell count)
- Low platelet count (thrombocytopenia)
- Elevated liver enzymes (detected on blood tests)
- Nausea or diarrhea
- Bruising or pain at the injection site
- Fever or swelling (edema)
- Shortness of breath (dyspnea) or confusion
Serious reactions — including spinal hematoma (bleeding around the spinal cord), severe allergic reactions, and significant internal bleeding — require emergency medical attention. Call 911 or go to the ER immediately if you experience sudden leg weakness, numbness, or loss of bladder/bowel control.
⚠️Warnings & precautions▾
Spinal/epidural hematoma (bleeding around the spinal cord) is the most critical risk. This can occur if you receive enoxaparin while having spinal anesthesia or a spinal tap, potentially causing long-term paralysis. The risk is higher with epidural catheters, certain other medications, or a history of spinal problems. Watch for sudden back pain, weakness, numbness, or loss of bladder/bowel control — and seek emergency care immediately.
- Bleeding risk: Enoxaparin increases the risk of bleeding throughout the body. Monitor for unusual bruising, prolonged bleeding, blood in urine or stool, or coughing/vomiting blood
- Heparin-induced thrombocytopenia (HIT): A rare but serious immune reaction that causes a dangerous drop in platelets and can paradoxically cause clots; enoxaparin must not be used in patients with a history of HIT within 100 days or with circulating HIT antibodies
- Not interchangeable: Enoxaparin cannot be swapped with regular heparin or other LMWHs without close medical supervision
- Mechanical heart valves in pregnancy: Pregnant women with mechanical prosthetic heart valves face an elevated risk of blood clots; extra monitoring and dose adjustment are required
- Kidney disease: Reduced kidney function slows clearance of enoxaparin, increasing bleeding risk; dose adjustment is needed for severe renal impairment
🔀What it interacts with▾
Several medications can increase the bleeding risk when taken with enoxaparin — tell your doctor and pharmacist about everything you take:
- Other anticoagulants (blood thinners): Adding another blood thinner significantly raises bleeding risk
- NSAIDs (ibuprofen, naproxen, ketorolac): These anti-inflammatory drugs affect platelet function and increase the chance of serious bleeding
- Aspirin and other salicylates: Even low-dose aspirin adds to bleeding risk; used intentionally in some cardiac indications, but always under medical supervision
- Platelet inhibitors (dipyridamole, clopidogrel, and similar drugs): These reduce platelet clotting and compound enoxaparin's effects
- Sulfinpyrazone (gout medication): Can enhance hemorrhage risk when combined with enoxaparin
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▾
- Active major bleeding: Enoxaparin is contraindicated — do not use it if you are currently having significant bleeding
- History of HIT (heparin-induced thrombocytopenia): Must not use enoxaparin if you had HIT within the last 100 days or have circulating HIT antibodies
- Allergies: Do not use if allergic to enoxaparin, heparin, pork products, or benzyl alcohol (the multiple-dose vial contains benzyl alcohol)
- Severe kidney disease: Dose adjustment is required; your prescriber needs to know your kidney function
- Pregnancy with mechanical heart valves: Significant added risk of clotting for mother and baby; requires intensive monitoring
- Upcoming spinal procedures or epidural anesthesia: Timing of enoxaparin doses must be carefully coordinated with your anesthesiologist and surgeon
- Older adults: May have reduced kidney clearance leading to higher drug exposure; prescribers should account for this
- Bleeding disorders: Patients should be evaluated for bleeding problems before starting enoxaparin
🚑If you take too much▾
Too much enoxaparin can lead to serious bleeding. If an overdose occurs, a medication called protamine sulfate can be given intravenously to partially reverse enoxaparin's effects — but it never fully neutralizes it, and it carries its own serious risks including severe low blood pressure and allergic reactions. Seek emergency medical care immediately if an overdose is suspected.
📡Pharmacodynamics — effects in the body▾
Enoxaparin slows the body's blood clotting system by strongly inhibiting Factor Xa (a key clotting protein) while having a lesser effect on thrombin (Factor IIa) — giving it a more targeted action than regular heparin. It measurably prolongs clotting times, including the activated partial thromboplastin time (aPTT), though the aPTT effect is more modest than with standard heparin. These combined effects reduce the blood's tendency to form dangerous clots while keeping clotting ability partially intact.
🔬Pharmacokinetics — how your body processes it▾
After a subcutaneous (under-the-skin) injection, enoxaparin reaches its peak blood-thinning activity in about 3 to 5 hours, and its effects last roughly 12 hours after a once-daily dose. It is processed mainly by the liver and cleared primarily through the kidneys, so people with reduced kidney function can have higher drug levels. The elimination half-life (the time for half the drug to leave the body) is approximately 4.5 hours after a single dose and up to about 7 hours with repeated dosing. When given intravenously, the drug acts more quickly, and steady drug levels in the blood are typically reached within the first 1 to 2 days of treatment.
📦How to store it▾
Store at 20° to 25°C (68° to 77°F); excursions permitted between 15° and 30°C (59° and 86°F). Store in the original carton or packaging until ready to use. Keep out of the reach of children.
📄 Written from Enoxaparin’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 Enoxaparin — the kind of thing our pharmacy team would talk through with you at the counter.
Why do I have to give myself shots instead of taking a pill? ▾
What should I watch for that means I need to call my doctor or go to the ER? ▾
Can I take ibuprofen or aspirin while I'm on this? ▾
Is it safe to have surgery or a spinal injection while I'm taking enoxaparin? ▾
I've heard this is similar to heparin. Can I switch between them? ▾
Does kidney disease affect how this medication works for me? ▾
Is Enoxaparin available over the counter? ▾
When was Enoxaparin first available? ▾
Who makes Enoxaparin? ▾
💬 Answers drafted from Enoxaparin’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 Enoxaparin comes
Enoxaparin 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
- Enoxaparin Sodium Injection and Lovenox are used to prevent DVT in patients having abdominal, hip, or knee replacement surgery, or in hospitalized patients with severely limited mobility
- Enoxaparin Sodium Injection and Lovenox are used to treat acute DVT with or without pulmonary embolism (inpatient), or DVT without pulmonary embolism (outpatient), given alongside warfarin
- Enoxaparin Sodium Injection and Lovenox are used to reduce the risk of ischemic complications in unstable angina and non-Q-wave myocardial infarction, given with aspirin
- Enoxaparin Sodium Injection and Lovenox are used to treat acute STEMI (a serious type of heart attack) managed medically or with percutaneous coronary intervention (PCI)
- Enoxaparin Sodium Injection and Lovenox are given by subcutaneous (under-the-skin) injection for most uses; an intravenous (IV) route is used for the initial dose in STEMI treatment
- Enoxiluv Kit contains enoxaparin sodium for subcutaneous injection — follow the specific instructions included with the kit
- Inject subcutaneously into the abdomen, thigh, or as directed; rotate injection sites to reduce bruising
- Timing of doses around surgical procedures or spinal interventions is critical — always follow your prescriber's specific schedule
Show 2 more strengths Show fewer strengths
📊 Enoxaparin across the U.S. market
How Enoxaparin 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 (8) — 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 Enoxaparin is used
A general measure of how commonly Enoxaparin 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 Enoxaparin 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 Enoxaparin prescribed? Of the 1,596 medications we measure, Enoxaparin ranks #343 by Medicaid prescriptions — more than 79% of them.
Utilization by Enoxaparin 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.
0.4 ML enoxaparin sodium 100 MG/ML Prefilled Syringe Most dispensed
Summed across the 19 of 53 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 854235
1 ML enoxaparin sodium 100 MG/ML Prefilled Syringe
Summed across the 14 of 48 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 854248
0.8 ML enoxaparin sodium 100 MG/ML Prefilled Syringe
Summed across the 12 of 49 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 854241
0.6 ML enoxaparin sodium 100 MG/ML Prefilled Syringe
Summed across the 14 of 48 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 854238
0.3 ML enoxaparin sodium 100 MG/ML Prefilled Syringe
Summed across the 15 of 48 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 854228
0.8 ML enoxaparin sodium 150 MG/ML Prefilled Syringe
Summed across the 13 of 46 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 854245
enoxaparin sodium 100 MG/ML Injectable Solution
Summed across the 7 of 13 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 854255
1 ML enoxaparin sodium 150 MG/ML Prefilled Syringe
Summed across the 9 of 46 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 854252
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 Enoxaparin, 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 103 of 351 listed Enoxaparin NDCs with Medicaid activity.
🔍 Compare Enoxaparin products
A representative set of FDA-listed product records for Enoxaparin — 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 | ||||
| 100 mg/mL | Subcutaneous | Amphastar Pharmaceuticals, Inc. × 20 listings | ANDA | View NDC → |
| 150 mg/mL | Subcutaneous | Amphastar Pharmaceuticals, Inc. × 8 listings | ANDA | View NDC → |
| 300 mg/3 mL | Intravenous, Subcutaneous | Amphastar Pharmaceuticals, Inc. | ANDA | View NDC → |
| 300 mg/3 mL | Intravenous; Subcutaneous | Amphastar Pharmaceuticals, Inc. × 2 listings | ANDA | View NDC → |
| 30 mg/0.3 mL | Subcutaneous | Apotex Corp. × 2 listings | ANDA | View NDC → |
| 40 mg/0.4 mL | Subcutaneous | Apotex Corp. × 2 listings | ANDA | View NDC → |
| 60 mg/0.6 mL | Subcutaneous | Apotex Corp. × 2 listings | ANDA | View NDC → |
| 80 mg/0.8 mL | Subcutaneous | Apotex Corp. × 2 listings | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | Apotex Corp. × 2 listings | ANDA | View NDC → |
| 120 mg/0.8 mL | Subcutaneous | Apotex Corp. × 2 listings | ANDA | View NDC → |
| 150 mg/mL | Subcutaneous | Apotex Corp. × 2 listings | ANDA | View NDC → |
| 30 mg/0.3 mL | Subcutaneous | BE Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 40 mg/0.4 mL | Subcutaneous | BE Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 60 mg/0.6 mL | Subcutaneous | BE Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 80 mg/0.8 mL | Subcutaneous | BE Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | BE Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 120 mg/0.8 mL | Subcutaneous | BE Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 150 mg/mL | Subcutaneous | BE Pharmaceuticals Inc. × 2 listings | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | BluePoint Laboratories × 15 listings | ANDA | View NDC → |
| 150 mg/mL | Subcutaneous | BluePoint Laboratories × 6 listings | ANDA | View NDC → |
| 300 mg/3 mL | Intravenous, Subcutaneous | BluePoint Laboratories × 2 listings | ANDA | View NDC → |
| 300 mg/3 mL | Intravenous; Subcutaneous | BluePoint Laboratories | ANDA | View NDC → |
| 30 mg/0.3 mL | Subcutaneous | Cardinal Health | ANDA | Find on DailyMed ↗ |
| 40 mg/0.4 mL | Intravenous; Subcutaneous | Cardinal Health | NDA | View NDC → |
| 40 mg/0.4 mL | Subcutaneous | Cardinal Health | ANDA | View NDC → |
| 60 mg/0.6 mL | Subcutaneous | Cardinal Health | ANDA | Find on DailyMed ↗ |
| 80 mg/0.8 mL | Subcutaneous | Cardinal Health | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | Cardinal Health × 6 listings | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | Cardinal Health | NDA AUTHORIZED GENERIC | Find on DailyMed ↗ |
| 40 mg/0.4 mL | Subcutaneous | Cardinal Health 107, LLC | NDA | View NDC → |
| 40 mg/0.4 mL | Subcutaneous | Cardinal Health 107, LLC × 2 listings | ANDA | View NDC → |
| 40 mg/0.4 mL | Intravenous; Subcutaneous | Cardinal Health 107, LLC | NDA | View NDC → |
| 80 mg/0.8 mL | Subcutaneous | Cardinal Health 107, LLC | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | Cardinal Health 107, LLC × 11 listings | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | Civica, Inc. | ANDA | View NDC → |
| 30 mg/0.3 mL | Subcutaneous | Fresenius Kabi USA, LLC × 6 listings | ANDA | View NDC → |
| 30 mg/0.3 mL | Subcutaneous | Fresenius Kabi USA, LLC × 5 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 40 mg/0.4 mL | Subcutaneous | Fresenius Kabi USA, LLC × 5 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 40 mg/0.4 mL | Subcutaneous | Fresenius Kabi USA, LLC × 6 listings | ANDA | View NDC → |
| 60 mg/0.6 mL | Subcutaneous | Fresenius Kabi USA, LLC × 5 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 60 mg/0.6 mL | Subcutaneous | Fresenius Kabi USA, LLC × 6 listings | ANDA | View NDC → |
| 80 mg/0.8 mL | Subcutaneous | Fresenius Kabi USA, LLC × 5 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 80 mg/0.8 mL | Subcutaneous | Fresenius Kabi USA, LLC × 6 listings | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | Fresenius Kabi USA, LLC × 6 listings | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | Fresenius Kabi USA, LLC × 6 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 120 mg/0.8 mL | Subcutaneous | Fresenius Kabi USA, LLC × 5 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 120 mg/0.8 mL | Subcutaneous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 150 mg/mL | Subcutaneous | Fresenius Kabi USA, LLC × 5 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 150 mg/mL | Subcutaneous | Fresenius Kabi USA, LLC × 3 listings | ANDA | View NDC → |
| 300 mg/3 mL | Intravenous, Subcutaneous | Fresenius Kabi USA, LLC × 2 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 300 mg/3 mL | Intravenous; Subcutaneous | Fresenius Kabi USA, LLC × 3 listings | NDA AUTHORIZED GENERIC | View NDC → |
| 30 mg/0.3 mL | Subcutaneous | Gland Pharma Limited × 2 listings | ANDA | View NDC → |
| 40 mg/0.4 mL | Subcutaneous | Gland Pharma Limited × 2 listings | ANDA | View NDC → |
| 60 mg/0.6 mL | Subcutaneous | Gland Pharma Limited × 2 listings | ANDA | View NDC → |
| 80 mg/0.8 mL | Subcutaneous | Gland Pharma Limited × 2 listings | ANDA | View NDC → |
| 100 mg/mL | Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 120 mg/0.8 mL | Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 150 mg/mL | Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
Showing 200 of 428 products — FDA National Drug Code Directory. See every product, package size and price: browse all 428 Enoxaparin 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 Enoxaparin — 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 Enoxaparin 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 Enoxaparin 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 67108 2 dose forms · 8 strengths
-
Dose form (SCDF) Injectable Solution RxCUI 372012In current FDA listingsClinical drug / strength (SCD) sodium 100 MG/MLRxCUI 854255 -
Dose form (SCDF) Prefilled Syringe RxCUI 727722No current FDA listingClinical drug / strength (SCD) 0.3 ML enoxaparin sodium 100 MG/MLRxCUI 8542280.4 ML enoxaparin sodium 100 MG/MLRxCUI 8542350.6 ML enoxaparin sodium 100 MG/MLRxCUI 8542380.8 ML enoxaparin sodium 100 MG/MLRxCUI 8542410.8 ML enoxaparin sodium 150 MG/MLRxCUI 8542451 ML enoxaparin sodium 100 MG/MLRxCUI 8542481 ML enoxaparin sodium 150 MG/MLRxCUI 854252
Look up RxCUI 67108 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 Enoxaparin 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
…and 6 more on the FDA NDC directory.
RxNorm drug class
Enoxaparin belongs to the Low Molecular Weight Heparin 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 30 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. Cardinal Health 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.