Nadolol, Bendroflumethiazide Oral Tablet 40-5Mg Drug Medication Dosage Information
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Nadolol, Bendroflumethiazide: Oral tablet (40-5mg)

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Drug Image file DrugItem_10102.JPG
Nadolol/Bendroflumeth 40-5 Tab
Global Pharmaceuticals
Pill Identification: G 531 

What is this Medicine?

BENDROFLUMETHIAZIDE; NADOLOL (ben droe floo meth EYE a zide; nay DOE lole) is a combination of a beta-blocker and a diuretic. It is used to treat high blood pressure.

CVS Pharmacy Patient Statistics for Nadolol, Bendroflumethiazide: Oral tablet(40-5mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information
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Nadolol/Bendroflumethiazide 40mg-5mg Tablet

NDC: 001155311
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Hypertension

Storage Information
Store at controlled room temperature (between 68 and 77 degrees F)
Nadolol/Bendroflumethiazide 40mg-5mg Tablet
Drug Image file DrugItem_10102.JPG
Global Pharmaceuticals
Pill Identification: G 531 
Shape: round
Color: white

Reported Side Effects for Nadolol/Bendroflumethiazide 40mg-5mg Tablet

Inflamed Pancreas Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Breathing Difficulties Incidence:
0.1%*
Severity: SEVERE
Onset: RAPID
Impotence (erectile Dysfunction) Incidence:
0.1-0.5%*
Severity: MODERATE
Onset: DELAYED
Decreased Sexual Desire Incidence:
0.1-0.5%*
Severity: MILD
Onset: DELAYED
Drowsiness Incidence:
0.6%*
Severity: MILD
Onset: EARLY
Paresthesias Incidence:
0.6%*
Severity: MILD
Onset: DELAYED
Low Blood Pressure Incidence:
1.0%*
Severity: MODERATE
Onset: RAPID
Heart Failure Incidence:
1.0%*
Severity: SEVERE
Onset: DELAYED
Lightheadedness Incidence:
2.0%*
Severity: MILD
Onset: EARLY
Slow Heart Beat Incidence:
2.0%*
Severity: SEVERE
Onset: RAPID
Peripheral Vasoconstriction Incidence:
2.0%*
Severity: MODERATE
Onset: RAPID
Tired Incidence:
2.0%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Daily Life Interactions for Nadolol/Bendroflumethiazide 40mg-5mg Tablet

Elements of your daily lifestyle may have an effect on the medications you are taking. Drug interactions can result in unwanted side effects, reduce the effectiveness of your medicine or possibly increase the action of a particular medicine.

Major Lifestyle Interaction
Marijuana and Nadolol/Bendroflumethiazide 40mg-5mg Tablet(Nadolol)
Marijuana and Beta-blockers(Nadolol)
Do not take Marijuana, Medical and Beta-Blockers (examples: Coreg, Metoprolol or Lopressor or Toprol, Nadolol or Corgard, Propranolol or Inderal) together without talking to your health care provider. Marijuana, Medical may decrease the effectiveness of Beta-Blockers. It is possible that Marijuana, Medical can cause high blood pressure, increased heart rate or other heart-related side effects in persons predisposed to these conditions, which may make the Beta-Blocker-type drug less effective at treating heart or blood pressure related problems.
Moderate Lifestyle Interaction
Alcohol and Nadolol/Bendroflumethiazide 40mg-5mg Tablet(Bendroflumethiazide)
Alcohol and Antihypertensives(Bendroflumethiazide)
Although an interaction is possible, Ethanol (alchohol) and Antihypertensive Agents (drugs used to reduce high blood pressure) may be used together. Ethanol or alchohol-containing beverages may increase the effects of Antihypertensive Agents on your blood pressure. If the blood pressure drops too low while taking Ethanol and Antihypertensive Agents, you may become dizzy or feel faint. To limit this interaction, avoid alcohol-containing beverages while taking medicines to lower your blood pressure. Do not stand or sit up too quickly. Contact your prescriber if you have dizziness which does not go away.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Avoid - This drug is known to cause harm to infants when taken by nursing mothers.


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