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Sacuvan 24 mg/26 mg Tablets

NAFDAC Reg. No. A4-100798 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Sacuvan 24 mg/26 mg Tablets
NAFDAC number
A4-100798
Active ingredient
Sacubitril; Valsartan
Strength
24 mg; 26 mg
Form
Tablet
Pack size
3 x 10's (in blisters)
Manufacturer
Not listed
Applicant (holder)
Hetero Labs Nigeria Limited
Approved
27 Mar 2024
Status
Active View on NAFDAC ↗
Registration valid to
26 Mar 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Sacuvan 24 mg/26 mg Tablets is on the NAFDAC register with an active registration (A4-100798). 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. This is not medical advice. Always follow your doctor or pharmacist.

What Sacuvan 24 mg/26 mg Tablets is used for

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

Boxed warning: FETAL TOXICITY When pregnancy is detected, discontinue ENTRESTO as soon as possible (5.1) Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus (5.1) WARNING: FETAL TOXICITY See full prescribing information for complete boxed warning. When pregnancy is detected, discontinue ENTRESTO as soon as possible. ( 5.1 ) Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. ( 5.1 )
What it is used for

ENTRESTO is a combination of sacubitril, a neprilisin inhibitor, and valsartan, an angiotensin II receptor blocker, and is indicated: to reduce the risk of cardiovascular death and hospitalization for heart failure in adult patients with chronic heart failure. Benefits are most clearly evident in patients with left ventricular ejection fraction (LVEF) below normal. ( 1.1 ) for the treatment of symptomatic heart failure with systemic left ventricular systolic dysfunction in pediatric patients aged one year and older. ENTRESTO reduces NT-proBNP and is expected to improve cardiovascular outcomes. …

Possible side effects

Clinically significant adverse reactions that appear in other sections of the labeling include: Angioedema [see Warnings and Precautions (5.2)] Hypotension [see Warnings and Precautions (5.3)] Impaired Renal Function [see Warnings and Precautions (5.4)] Hyperkalemia [see Warnings and Precautions (5.5)] Adverse reactions occurring greater than or equal to 5% are hypotension, hyperkalemia, cough, dizziness, and renal failure. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Novartis Pharmaceuticals Corporation at 1-888-669-6682 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . …

Do not use if

ENTRESTO is contraindicated: in patients with hypersensitivity to any component in patients with a history of angioedema related to previous ACE inhibitor or ARB therapy [see Warnings and Precautions (5.2)] with concomitant use of ACE inhibitors. Do not administer within 36 hours of switching from or to an ACE inhibitor [see Drug Interactions (7.1)] with concomitant use of aliskiren in patients with diabetes [see Drug Interactions (7.1)] Hypersensitivity to any component. …

Warnings

Observe for signs and symptoms of angioedema and hypotension. ( 5.2 , 5.3 ) Monitor renal function and potassium in susceptible patients. ( 5.4 , 5.5 ) 5.1 Fetal Toxicity ENTRESTO can cause fetal harm when administered to a pregnant woman. Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death. When pregnancy is detected, consider alternative drug treatment and discontinue ENTRESTO. …

Pregnancy & breastfeeding

8.1 Pregnancy Risk Summary ENTRESTO can cause fetal harm when administered to a pregnant woman. Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death ( see Clinical Considerations ). …

Storage

Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C and 30°C (59°F and 86°F) [see USP Controlled Room Temperature]. Protect from moisture.

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

Check your pack of Sacuvan 24 mg/26 mg Tablets

Add the expiry date on your pack for a full Trust Score.

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Sacuvan 24 mg/26 mg Tablets

What is in Sacuvan 24 mg/26 mg Tablets?

Sacuvan 24 mg/26 mg Tablets contains Sacubitril; Valsartan (24 mg; 26 mg), as tablet, according to its NAFDAC registration record.

Is Sacuvan 24 mg/26 mg Tablets registered with NAFDAC?

Yes. Sacuvan 24 mg/26 mg Tablets is listed on the NAFDAC register under registration number A4-100798, and its registration is active as of 27 October 2026.

Has Sacuvan 24 mg/26 mg Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Sacuvan 24 mg/26 mg Tablets in our automatically synced alert list.

How can I check that my pack of Sacuvan 24 mg/26 mg Tablets is genuine?

Run a free authenticity scan with the NAFDAC number A4-100798, 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 Sacuvan 24 mg/26 mg Tablets used for?

ENTRESTO is a combination of sacubitril, a neprilisin inhibitor, and valsartan, an angiotensin II receptor blocker, and is indicated: to reduce the risk of cardiovascular death and hospitalization for heart failure in adult patients with chronic heart failure. Benefits are most clearly evident in patients with left ventricular ejection fraction (LVEF) below normal. ( 1.1 ) for the treatment of sym (Summarised from the official U.S. FDA label for sacubitril. Always follow your doctor or pharmacist.)

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