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Metoprolol 50 mg Tablets

NAFDAC Reg. No. C4-1616 · Drug

Registered with NAFDAC. Registration activeAs of 29 October 2026 · synced automatically from official sources.
Product
Metoprolol 50 mg Tablets
NAFDAC number
C4-1616
Active ingredient
Metoprolol Tartrate (Metoprolol Succinate)
Strength
50 mg
Form
Tablet
Pack size
2 x 14's (in PVC-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
Anyi-Tex Pharmaceuticals Limited
Approved
25 Feb 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
24 Feb 2026
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Metoprolol tartrate: uses, dosage and brands worldwide

What we found

  • Metoprolol 50 mg Tablets is on the NAFDAC register with an active registration (C4-1616). 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.

How to use Metoprolol 50 mg Tablets

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

Metoprolol tartrate tablets are a beta-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Angina Pectoris. ( 1.2 ) Myocardial Infarction, to reduce the risk of cardiovascular mortality when used in conjunction with intravenous metoprolol therapy in patients with definite or suspected acute myocardial infarction in hemodynamically stable patients. ( 1.3 ) 1.1 Hypertension Metoprolol tartrate tablets are indicated for the treatment of hypertension in adult patients, to lower blood pressure. …

How to take it and how often
  • Administer once daily with food or after a meal
  • Titrate at weekly or longer intervals as needed and tolerated
  • Hypertension: Recommended starting dosage is 100 mg daily, in single or divided doses
  • Angina Pectoris: Recommended starting dosage is 100 mg daily, given as two divided doses
  • Myocardial Infarction: The starting dosage depends upon tolerance of intravenous metoprolol, see full prescribing information
  • Hypertension Individualize the dosage of metoprolol tartrate tablets
  • Metoprolol tartrate tablets should be taken with or immediately following meals
  • The usual initial dosage is 100 mg daily in single or divided doses
  • Adjust dosage at weekly (or longer) intervals until optimum blood pressure reduction is achieved
  • In general, the maximum effect of any given dosage level will be apparent after 1 week of therapy
  • The effective dosage range of metoprolol tartrate tablets is 100 mg to 450 mg per day
  • Dosages above 450 mg per day have not been studied
  • While once-daily dosing can maintain a reduction in blood pressure throughout the day, lower doses (especially 100 mg) may not maintain a full effect at the end of the 24-hour period
  • Larger or more frequent daily doses may be required
Strengths it comes in

Metoprolol tartrate tablets, USP are supplied as: 25 mg tablet – white round shaped, film coated tablets debossed with ‘C over 73’ on one side and deep break line on other side. 50 mg tablet – pink round shaped, film coated tablets debossed with ‘C over 74’ on one side and deep break line on other side. …

Children
  • Safety and effectiveness of metoprolol have not been established
  • In pediatric patients
Older adults

Clinical studies of metoprolol in hypertension did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience in hypertensive patients has not identified differences in responses between elderly and younger patients. …

While you are taking it
  • Advise patients to take metoprolol tartrate tablets regularly and continuously, as directed, preferably with or immediately following meals
  • If a dose is missed, the patient should take only the next scheduled dose (without doubling it)
  • Patients should not interrupt or discontinue metoprolol tartrate tablets without consulting the physician
  • Advise patients to avoid operating automobiles and machinery or engaging in other tasks requiring alertness until the patient’s response to therapy with metoprolol tartrate tablets has been determined; to contact the physician if any difficulty in breathing occurs; to inform the physician or dentist before any type of surgery that he or she …
Talk to a doctor first if

Metoprolol tartrate tablets are contraindicated in severe bradycardia, second- or third-degree heart block, cardiogenic shock, systolic blood pressure

Medicines it may not mix with

Catecholamine-depleting drugs may have an additive effect when given with beta-blocking agents. ( 7.1 ) Patients may be unresponsive to the usual doses of epinephrine used to treat allergic reaction. ( 7.2 ) CYP2D6 Inhibitors are likely to increase metoprolol concentration. ( 7.3 ) Concomitant use of glycosides, clonidine, and diltiazem and verapamil with beta-blockers can increase the risk of bradycardia. ( 7.4 ) Beta-blockers including metoprolol, may exacerbate the rebound hypertension that can follow the withdrawal of clonidine. …

Warnings

Abrupt cessation may exacerbate myocardial ischemia. ( 5.1 ) Heart Failure: Worsening cardiac failure may occur. ( 5.2 ) Bronchospastic Disease: Avoid beta-blockers. ( 5.3 ) Pheochromocytoma: Initiate therapy with an alpha blocker. ( 5.4 ) Major Surgery: Avoid initiation of high-dose extended-release metoprolol in patients undergoing non-cardiac surgery. Do not routinely withdraw chronic beta-blocker therapy prior to surgery. ( 5.5 , 6.1 ) Diabetes: May mask symptoms of hypoglycemia.( 5.6 ) Thyrotoxicosis: Abrupt withdrawal in patients with thyrotoxicosis might precipitate a thyroid storm. ( 5.7 ) Peripheral Vascular Disease: Can aggravate symptoms of arterial insufficiency. …

Possible side effects

The following adverse reactions are described elsewhere in labeling: Worsening angina or myocardial infarction [see Warnings and Precautions (5) ] Worsening heart failure [see Warnings and Precautions (5) ]. Worsening AV block [see Contraindications (4) ]. ­Most common adverse reactions: tiredness, dizziness, depression, shortness of breath, bradycardia, hypotension, diarrhea, pruritus, rash. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Rising Pharma Holdings, Inc. at 1-844-874-7464 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Available data from published observational studies have not demonstrated an association of adverse developmental outcomes with maternal use of metoprolol during pregnancy ( see Data). Untreated hypertension and myocardial infarction during pregnancy can lead to adverse outcomes for the mother and the fetus (see Clinical Considerations). …

If you take too much

Signs and Symptoms - Overdosage of metoprolol may lead to severe bradycardia, hypotension, and cardiogenic shock. Clinical presentation can also include: atrioventricular block, heart failure, bronchospasm, hypoxia, impairment of consciousness/coma, nausea and vomiting. Treatment – Consider treating the patient with intensive care. Patients with myocardial infarction or heart failure may be prone to significant hemodynamic instability. Beta-blocker overdose may result in significant resistance to resuscitation with adrenergic agents, including beta-agonists. …

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-06-10.

Label for metoprolol tartrate (metoprolol succinate), the active ingredient registered with NAFDAC.

Check your pack of Metoprolol 50 mg Tablets

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

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Metoprolol 50 mg Tablets

What is in Metoprolol 50 mg Tablets?

Metoprolol 50 mg Tablets contains Metoprolol Tartrate (Metoprolol Succinate) (50 mg), as tablet, according to its NAFDAC registration record.

Is Metoprolol 50 mg Tablets registered with NAFDAC?

Yes. Metoprolol 50 mg Tablets is listed on the NAFDAC register under registration number C4-1616, and its registration is active as of 29 October 2026.

Has Metoprolol 50 mg Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Metoprolol 50 mg Tablets in our automatically synced alert list.

How can I check that my pack of Metoprolol 50 mg Tablets is genuine?

Run a free authenticity scan with the NAFDAC number C4-1616, 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.

How do I take Metoprolol 50 mg Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Administer once daily with food or after a meal. Titrate at weekly or longer intervals as needed and tolerated. ( 2 ) Hypertension: Recommended starting dosage is 100 mg daily, in single or divided doses. ( 2.1 ) Angina Pectoris: Recommended starting dosage is 100 mg daily, given as two divided doses. ( 2.2 ) Myocardial Infarction: The starting dosage depends upon tolerance of …

What is Metoprolol 50 mg Tablets used for?

Metoprolol tartrate tablets are a beta-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Angina Pectoris. ( 1.2 ) Myocardial Infarction, to reduce the risk of cardiovascular mortality when used in conjunction with intra (Summarised from the official U.S. FDA label for metoprolol tartrate (metoprolol succinate). Always follow your doctor or pharmacist.)

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