Valsartan: uses, dosing, side effects & brands
Valsartan is an angiotensin 2 receptor blocker sold in the U.S. under 2 brand and generic names, for diabetic nephropathies, heart failure and hypertension. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.
Key facts
- Drug class
- Angiotensin 2 Receptor Blocker
- Treats
- Diabetic Nephropathies, Heart Failure and Hypertension
- Available as
- Tablet
- Sold as
- 2 products — Diovan and Valsartan
- Prescription?
- Prescription only
- Generic available?
- Yes
- What the pharmacy pays
- about $4 for a 30-count supply — not your price
- Boxed warning
- Boxed warning
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How valsartan is dosed
From the FDA label for Valsartan (application ANDA204011). Other valsartan products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.
Indication Starting Dose Dose Range Target Maintenance Dose* Adult Hypertension ( 2.1 ) 80 mg or 160 mg once daily 80 mg to 320 mg once daily --- Pediatric Hypertension (6 to 16 years) ( 2.2 ) 1.3 mg/kg once daily (up to 40 mg total) 1.3 mg/kg to 2.7 mg/kg once daily (up to 40 mg to 160 mg total) --- Heart Failure ( 2.3 ) 40 mg twice daily 40 mg to 160 mg twice daily 160 mg twice daily Post-Myocardial Infarction (2.4) 20 mg twice daily 20 mg to 160 mg twice daily 160 mg twice daily * as tolerated by patient 2.1 Adult Hypertension The recommended starting dose of valsartan tablets is 80 mg or 160 mg once daily when used as monotherapy in patients who are not volume-depleted. Patients requiring greater reductions may be started at the higher dose. Valsartan tablets may be used over a dose range of 80 mg to 320 mg daily, administered once a day. The antihypertensive effect is substantially present within 2 weeks and maximal reduction is generally attained after 4 weeks. If additional antihypertensive effect is required over the starting dose range, the dose may be increased to a maximum of 320 mg or a diuretic may be added. Addition of a diuretic has a greater effect than dose increases beyond 80 mg. Valsartan tablets may be administered with other antihypertensive agents. 2.2 Pediatric Hypertension 6 to 16 Years of Age For pediatric patients who can swallow tablets, the usual…
Valsartan side effects
Hypertension: Most common adverse reactions are headache, dizziness, viral infection, fatigue and abdominal pain. (6.1) Heart Failure: Most common adverse reactions are dizziness, hypotension, diarrhea, arthralgia, back pain, fatigue and hyperkalemia. (6.1) Post-Myocardial Infarction: Most common adverse reactions which caused patients to discontinue therapy are hypotension, cough and increased blood creatinine. (6.1) To report SUSPECTED ADVERSE REACTIONS, contact AvKARE at 1-855-361-3993 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Studies Experience Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect the rates observed in practice. Adult Hypertension Valsartan has been evaluated for safety in more than 4,000 patients, including over 400 treated for over 6 months, and more than 160 for over 1 year. Adverse reactions have generally been mild and transient in nature and have only infrequently required discontinuation of therapy. The overall incidence of adverse reactions with valsartan was similar to placebo. The overall frequency of adverse reactions was neither dose-related nor related to gender, age, race, or regimen. Discontinuation of therapy due to side effects was required…
Who shouldn’t take valsartan
Do not use in patients with known hypersensitivity to any component. Do not co-administer aliskiren with valsartan tablets in patients with diabetes [see Drug Interactions (7) ] . Known hypersensitivity to any component. Do not co-administer aliskiren with valsartan tablets in patients with diabetes. (4)
Valsartan drug interactions
Potassium-sparing diuretics, potassium supplements or salt substitutes may lead to increases in serum potassium, and in heart failure patients, increases in serum creatinine. (7.1) NSAID use may lead to increased risk of renal impairment and loss of antihypertensive effect. (7.2) Dual inhibition of the renin-angiotensin system: Increased risk of renal impairment, hypotension, and hyperkalemia. (7.3) Lithium: Increases in serum lithium level and lithium toxicity. (7.4) 7.1 Agents Increasing Serum Potassium Concomitant use of valsartan with other agents that block the renin-angiotensin system, potassium-sparing diuretics (e.g., spironolactone, triamterene, amiloride), potassium supplements, salt substitutes containing potassium or other drugs that may increase potassium levels (e.g., heparin) may lead to increases in serum potassium and in heart failure patients to increases in serum creatinine. If co-medication is considered necessary, monitoring of serum potassium is advisable. 7.2 Non-Steroidal Anti-Inflammatory Agents Including Selective Cyclooxygenase-2 Inhibitors (COX-2 Inhibitors) In patients who are elderly, volume-depleted (including those on diuretic therapy), or with compromised renal function, co-administration of NSAIDs, including selective COX-2 inhibitors, with angiotensin II receptor antagonists, including valsartan, may result in deterioration of renal function, including possible acute renal failure. These effects are usually reversible. Monitor renal function periodically in patients receiving valsartan and NSAID therapy. The antihypertensive effect of angiotensin II receptor antagonists, including valsartan, may be attenuated by NSAIDs including selective COX-2 inhibitors. 7.3 Dual Blockade of the Renin-Angiotensin System (RAS) Dual blockade of the RAS with angiotensin receptor blockers, ACE inhibitors, or aliskiren is associated with increased risks of hypotension, hyperkalemia, and changes in renal function (including acute renal failure) compared to monotherapy. Most patients receiving the combination of two RAS inhibitors do not obtain any additional benefit compared to monotherapy [see Clinical Studies (14.3) ] . In general, avoid combined use of RAS inhibitors. Closely monitor blood pressure, renal function and electrolytes in patients on valsartan and other agents that affect the RAS. Do not co-administer aliskiren with valsartan in patients with diabetes. Avoid use of aliskiren with valsartan in patients with renal impairment (GFR < 60 mL/min). 7.4 Lithium Increases in serum lithium concentrations and lithium toxicity have been reported during concomitant administration of lithium with angiotensin II receptor antagonists. Monitor serum lithium levels during concomitant use.
Valsartan and food
Potassium-rich foods & salt substitutes
Don't use potassium-based salt substitutes unless your clinician approves, and ask before taking potassium supplements. Your clinician may check your potassium level with blood tests.
Lisinopril (an ACE inhibitor) — MedlinePlus (U.S. National Library of Medicine) ↗
Every valsartan product we track (2)
Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.
| # | Drug | Rating | Type | Form | Generic? | Pharmacy pays | |
|---|---|---|---|---|---|---|---|
| 1 | 70/100 | Prescription | Tablet | Generic | $4 | View → | |
| 2 | 70/100 | Prescription | Tablet | Generic | $4 | View → |
What valsartan pills look like
Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.
| Imprint | Strength | Colour | Shape | Maker |
|---|---|---|---|---|
| H;184 | 160 mg | yellow | oval | — |
| 40 | 40 mg | yellow | capsule | — |
| P;172 | 5 mg / 160 mg / 12.5 mg | white | oval | — |
| P;174 | 10 mg / 160 mg / 12.5 mg | brown | oval | — |
| P;173 | 5 mg / 160 mg / 25 mg | yellow | oval | — |
| P;175 | 10 mg / 25 mg / 320 mg | white | oval | — |
| P;185 | 10 mg / 25 mg / 160 mg | yellow | oval | — |
| P;172 | 5 mg / 160 mg / 12.5 mg | white | oval | — |
| P;174 | 10 mg / 160 mg / 12.5 mg | brown | oval | — |
| P;173 | 5 mg / 160 mg / 25 mg | yellow | oval | — |
| P;175 | 10 mg / 25 mg / 320 mg | white | oval | — |
| P;185 | 10 mg / 25 mg / 160 mg | yellow | oval | — |
Combination products containing valsartan
A combination is a different drug — different dosing, different warnings. It is listed here so you can find it, not so you can substitute it.
Valsartan recalls
From the FDA Enforcement database. A recall covers specific lots — not the drug as a whole.
How long valsartan keeps
No valsartan label we read sets a separate limit for after opening, but they do specify how it must be stored — and the stability behind any date assumes those conditions.
Does valsartan expire? The in-use limits and storage rules from its labelsValsartan and breastfeeding
From LactMed, the US National Library of Medicine’s Drugs and Lactation Database — quoted, not rewritten.
Full LactMed record for valsartan: levels in milk, effects in breastfed infants, and the drugs it would consider insteadMilk levels after the lowest dose of the combination of valsartan and sacubitril (Entresto) are very low. If the highest recommended maternal dosage (6 times greater) produces proportionate milk levels, they would likely still be quite low. Valsartan is unlikely to affect the nursing infant.
National Institute of Child Health and Human Development, record revised November 15, 2024. LactMed states its information is not a substitute for professional judgement.
What people report to the FDA about valsartan
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 76,613 reports naming valsartan, and the FDA flagged 79% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- fatigue4,248 reports
- dyspnoea4,216 reports
- dizziness4,054 reports
- nausea3,883 reports
- diarrhoea3,668 reports
- headache3,306 reports
- acute kidney injury3,245 reports
- hypotension2,816 reports
Read these as a signal, not a rate. A report does not mean valsartan caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label section above.
Source: openFDA drug/event (FAERS), retrieved August 26, 2026.
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Frequently asked questions
What is valsartan?
Valsartan is an angiotensin 2 receptor blocker used to treat Diabetic Nephropathies, Heart Failure, Hypertension, Left Ventricular Dysfunction.
What kind of drug is valsartan?
The FDA classifies valsartan as an angiotensin 2 receptor blocker. Angiotensin II receptor blockers (ARBs) block the AT1 receptor that the hormone angiotensin II uses to tighten blood vessels and make the body hold onto salt and water. With that receptor blocked, vessels relax and widen, so blood pressure falls. If you are checking whether it is safe to combine with something else, the class is what matters — two drugs from the same class usually should not be stacked.
Can you take valsartan with other medicines?
It depends on the medicine. We check it against the FDA labels rather than guessing: our interaction checker searches each drug's own label for the other and quotes what it says, naming the section it came from. Run valsartan against whatever else you take — and remember that a label not naming a drug is not the same as that combination being safe.
What brand names is valsartan sold under?
We track 2 valsartan-containing products in the U.S.: Diovan and Valsartan. They are the same active ingredient; they differ in form, manufacturer, price and FDA recall record.
What forms does valsartan come in?
Across the brands we track, valsartan is currently marketed as tablet, per the FDA's National Drug Code Directory. Each form is dosed differently — follow the label for the exact product you were prescribed.
Is there a generic valsartan?
Yes. Our catalog lists 1 generic valsartan product alongside the brand versions. A generic has the same active ingredient and must meet the FDA's bioequivalence standard; it usually costs less. Ask your pharmacist which one your plan covers.
Has valsartan been recalled?
The FDA's Enforcement database lists 1 recall record whose product description mentions valsartan. The most recent: Diovan (valsartan) 160 mg (Aug 4, 2026). A recall applies to specific lots, not to the drug as a whole — check the record for the affected lot numbers.
What should I avoid while taking valsartan?
Food: salt substitutes containing potassium, and large amounts of potassium-rich foods or supplements — see the food section above for what each one does and whether it means avoiding it or just being consistent. This is what the FDA label and our cited sources say — it is not a complete list. Your pharmacist can check your own combination.
Cite this page
- APA
- pharmaranks. (2026, July 24). Valsartan: uses, dosing, side effects & brands. https://pharmaranks.com/drugs/valsartan
- MLA
- “Valsartan: uses, dosing, side effects & brands.” pharmaranks, 24 July 2026, https://pharmaranks.com/drugs/valsartan.
We summarise public FDA and NIH sources — for a clinical claim, cite the primary source we link to as well.
Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.
Read the full FDA label for valsartan on DailyMed (NIH) ↗ — including its boxed warning in full.