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Clexane Injectable Solution 6000 IU

NAFDAC Reg. No. A6-0463 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Clexane Injectable Solution 6000 IU
NAFDAC number
A6-0463
Active ingredient
Enoxaparin Sodium
Strength
60 mg/0.6 mL
Form
Solution for injection
Pack size
0.6 mL x 2’s (in Pre-Filled Syringes)
Manufacturer
Not listed
Applicant (holder)
Sanofi-Aventis Nigeria Limited
Approved
26 Feb 2023
Status
Active View on NAFDAC ↗
Registration valid to
25 Feb 2028
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Clexane Injectable Solution 6000 IU is on the NAFDAC register with an active registration (A6-0463). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.

What Clexane Injectable Solution 6000 IU is used for

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

Boxed warning: SPINAL/EPIDURAL HEMATOMAS Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures. …
What it is used for

Enoxaparin sodium injection is a low molecular weight heparin (LMWH) indicated for: Prophylaxis of deep vein thrombosis (DVT) in abdominal surgery, hip replacement surgery, knee replacement surgery, or medical patients with severely restricted mobility during acute illness ( 1.1 ) Inpatient treatment of acute DVT with or without pulmonary embolism ( 1.2 ) Outpatient treatment of acute DVT without pulmonary embolism ( 1.2 ) Prophylaxis of ischemic complications of unstable angina and non−Q-wave myocardial infarction (MI) ( 1.3 ) Treatment of acute ST-segment elevation myocardial infarction (STEMI) managed medically or with subsequent percutaneous coronary intervention (PCI) ( 1.4 ) 1.1 Prophy …

Possible side effects

The following serious adverse reactions are also discussed in other sections of the labeling: • Spinal/epidural hematomas [see Boxed Warning and Warnings and Precautions ( 5.1 )] • Increased Risk of Hemorrhage [see Warnings and Precautions ( 5.1 )] • Thrombocytopenia [see Warnings and Precautions ( 5.5 )] Most common adverse reactions (>1%) were bleeding, anemia, thrombocytopenia, elevation of serum aminotransferase, diarrhea, nausea, ecchymosis, fever, edema, peripheral edema, dyspnea, confusion, and injection site pain ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact NorthStar at 1-800-206-7821 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. …

Do not use if

Enoxaparin sodium injection is contraindicated in patients with: • Active major bleeding • History of immune-mediated heparin-induced thrombocytopenia (HIT) within the past 100 days or in the presence of circulating antibodies [see Warnings and Precautions (5.4) ] • Known hypersensitivity to enoxaparin sodium (e.g., pruritus, urticaria, anaphylactic/ anaphylactoid reactions) [see Adverse Reactions (6.2) ] • Known hypersensitivity to heparin or pork products Active major bleeding ( 4 ) History of …

Warnings

Increased risk of hemorrhage: Monitor for signs of bleeding ( 5.1 , 5.2 , 5.3 ) Risk of Heparin-Induced Thrombocytopenia with or without Thrombosis ( 5.4 ) Thrombocytopenia: Monitor platelet count closely ( 5.5 ) Interchangeability with other heparins: Do not exchange with heparin or other LMWHs ( 5.6 ) Increased Risk of Thrombosis in Pregnant women with Mechanical Prosthetic Heart Valves: women and their fetuses may be at increased risk. Monitor more frequently and adjust dosage as needed. …

Pregnancy & breastfeeding

8.1 Pregnancy Risk Summary Placental transfer of enoxaparin was observed in the animal studies. Human data from a retrospective cohort study, which included 693 live births, suggest that enoxaparin sodium does not increase the risk of major developmental abnormalities [see Data]. Based on animal data, enoxaparin is not predicted to increase the risk of major developmental abnormalities [see Data]. …

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

Check your pack of Clexane Injectable Solution 6000 IU

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Clexane Injectable Solution 6000 IU

What is in Clexane Injectable Solution 6000 IU?

Clexane Injectable Solution 6000 IU contains Enoxaparin Sodium (60 mg/0.6 mL), as solution for injection, according to its NAFDAC registration record.

Is Clexane Injectable Solution 6000 IU registered with NAFDAC?

Yes. Clexane Injectable Solution 6000 IU is listed on the NAFDAC register under registration number A6-0463, and its registration is active as of 6 November 2026.

Has Clexane Injectable Solution 6000 IU been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Clexane Injectable Solution 6000 IU in our automatically synced alert list.

How can I check that my pack of Clexane Injectable Solution 6000 IU is genuine?

Run a free authenticity scan with the NAFDAC number A6-0463, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Clexane Injectable Solution 6000 IU used for?

Enoxaparin sodium injection is a low molecular weight heparin (LMWH) indicated for: Prophylaxis of deep vein thrombosis (DVT) in abdominal surgery, hip replacement surgery, knee replacement surgery, or medical patients with severely restricted mobility during acute illness ( 1.1 ) Inpatient treatment of acute DVT with or without pulmonary embolism ( 1.2 ) Outpatient treatment of acute DVT without (Summarised from the official U.S. FDA label for enoxaparin sodium. Always follow your doctor or pharmacist.)

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