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Sodium citrate

Sildenafil tablets are indicated for the treatment of erectile dysfunction. Sildenafil is a phosphodiesterase-5 (PDE5) inhibitor indicated for the tre.

Prescription medicine Oral Safety alerts on record

How to use Sodium citrate

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

Sildenafil tablets are indicated for the treatment of erectile dysfunction. Sildenafil is a phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED)

How to take it and how often
  • For most patients, the recommended dose is 50 mg taken, as needed, approximately 1 hour before sexual activity
  • However, sildenafil tablets may be taken anywhere from 30 minutes to 4 hours before sexual activity Based on effectiveness and toleration, may increase to a maximum of 100 mg or decrease to 25 mg Maximum recommended dosing frequency is once per day Dosage Information For most patients, the recommended dose is 50 mg taken, as needed, approximately 1 hour before sexual activity
  • However, sildenafil tablets may be taken anywhere from 30 minutes to 4 hours before sexual activity
  • The maximum recommended dosing frequency is once per day
  • Based on effectiveness and toleration, the dose may be increased to a maximum recommended dose of 100 mg or decreased to 25 mg
  • Use with Food Sildenafil tablets may be taken with or without food
  • Dosage Adjustments in Specific Situations Sildenafil tablets was shown to potentiate the hypotensive effects of nitrates and its administration in patients who use nitric oxide donors such as organic nitrates or organic nitrites in any form is therefore contraindicated [ see Contraindications , Drug Interactions , and Clinical Pharmacology ]
  • When sildenafil tablets are co-administered with an alpha-blocker, patients should be stable on alpha-blocker therapy prior to initiating sildenafil tablets treatment and sildenafil tablets should be initiated at 25 mg [ see Warnings and Precautions , Drug Interactions , and Clinical Pharmacology ]. …
Strengths it comes in

Sildenafil tablets, USP are supplied as pale blue to blue, caplet shaped film-coated tablets containing sildenafil citrate USP equivalent to 50 mg, or 100 mg of sildenafil. Tablets are debossed with 1A1 and 1A2 on one side and plain on the other to indicate the dosage strengths viz. 100 mg and 50 mg respectively. …

Children
  • Sildenafil is not indicated for use
  • In pediatric patients
  • Safety and effectiveness have not been established
  • In pediatric patients
Older adults

Healthy elderly volunteers (65 years or over) had a reduced clearance of sildenafil resulting in approximately 84% and 107% higher plasma AUC values of sildenafil and its active N-desmethyl metabolite, respectively, compared to those seen in healthy young volunteers (18-45 years) [ see Clinical Pharmacology (12.3) ]. …

While you are taking it
  • Advise the patient to read the FDA-approved patient labeling (Patient Information) Nitrates Physicians should discuss with patients the contraindication of sildenafil with regular and/or intermittent use of nitric oxide donors, such as organic nitrates or organic nitrites in any form [ see Contraindications ]
  • Guanylate Cyclase (GC) Stimulators Physicians should discuss with patients the contraindication of sildenafil with use of guanylate cyclase stimulators such as riociguat [ see Contraindications ]. …
Talk to a doctor first if
  • Administration of sildenafil tablets to patients using nitric oxide donors, such as organic nitrates or organic nitrites in any form
  • Sildenafil tablets was shown to potentiate the hypotensive effect of nitrates Known hypersensitivity to sildenafil or any component of tablet Administration with guanylate cyclase (GC) stimulators, such as riociguat Nitrates Consistent with its known effects on the nitric oxide/cGMP pathway [ see Clinical Pharmacology (12.1 …
Medicines it may not mix with

Sildenafil can potentiate the hypotensive effects of nitrates, alpha blockers, and anti-hypertensives ( 4.1 , 5.5 , 7.1 , 7.2 , 7.3 , 12.2 ) With concomitant use of alpha blockers, initiate sildenafil at 25 mg dose ( 2.3 ) CYP3A4 inhibitors (e.g., ritonavir, ketoconazole, itraconazole, erythromycin): Increase sildenafil exposure ( 2.4 , 7.4 , 12.3 ) Ritonavir: Do not exceed a maximum single dose of 25 mg in a 48 hour period ( 2.4 , 5.6 ) Erythromycin or strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole, saquinavir): Consider a starting dose of 25 mg ( 2.4 , 7.4 ) 7.1 Nitrates Administration of sildenafil with nitric oxide donors such as organic nitrates or organic nitrites in any fo …

Warnings

Patients should not use sildenafil if sexual activity is inadvisable due to cardiovascular status ( 5.1 ) Patients should seek emergency treatment if an erection lasts >4 hours. Use sildenafil with caution in patients predisposed to priapism ( 5.2 ) Patients should stop sildenafil tablets and seek medical care if a sudden loss of vision occurs in one or both eyes, which could be a sign of non arteritic anterior ischemic optic neuropathy (NAION). Sildenafil tablets should be used with caution, and only when the anticipated benefits outweigh the risks, in patients with a history of NAION. Patients with a "crowded" optic disc may also be at an increased risk of NAION. …

Possible side effects

The following are discussed in more detail in other sections of the labeling: Cardiovascular [ see Warnings and Precautions (5.1) ] Prolonged Erection and Priapism [ see Warnings and Precautions (5.2) ] Effects on the Eye [ see Warnings and Precautions (5.3) ] Hearing Loss [ see Warnings and Precautions (5.4) ] Hypotension when Co-administered with Alpha-blockers or Anti-hypertensives [ see Warnings and Precautions (5.5) ] Adverse Reactions with the Concomitant Use of Ritonavir [ see Warnings and Precautions (5.6) ] Combination with other PDE5 Inhibitors or Other Erectile Dysfunction Therapies [ see Warnings and Precautions (5.7) ] Effects on Bleeding [ see Warnings and Precautions (5.8) ] C …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Sildenafil is not indicated for use in females. There are no data with the use of sildenafil in pregnant women to inform any drug-associated risks for adverse developmental outcomes. Animal reproduction studies conducted with sildenafil did not show adverse developmental outcomes when administered during organogenesis in rats and rabbits at oral doses up to 16 and 32 times, respectively, the maximum recommended human do …

If you take too much

In studies with healthy volunteers of single doses up to 800 mg, adverse reactions were similar to those seen at lower doses but incidence rates and severities were increased. In cases of overdose, standard supportive measures should be adopted as required. Renal dialysis is not expected to accelerate clearance as sildenafil is highly bound to plasma proteins and it is not eliminated in the urine.

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 2026-07-29.

Brands around the world

Products with Sodium citrate as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

Sodium Citrate W/v AnticoagulantTRISODIUM CITRATE DIHYDRATE 4 g/100mL · Injection, Solution · Terumo BCT, Ltd
NDC 14537-883Label
Acd A ADEXTROSE MONOHYDRATE 2.45 g/100mL, SODIUM CITRATE, UNSPECIFIED FORM 2.2 g/100mL, CITRIC ACID MONOHYDRATE .8 g/100mL · Injection, Solution · Terumo BCT Ltd
NDC 14537-967Label
Anticoagulant Sodium CitrateTRISODIUM CITRATE DIHYDRATE 40 mg/mL · Solution · Baxter Healthcare Corporation
NDC 0338-9669Label
Emetrol Chewables OrangeTRISODIUM CITRATE DIHYDRATE 230 mg/1 · Tablet, Chewable · WellSpring Pharmaceutical Corporation
NDC 65197-410Label
Walgreens Upset Stomach And Nausea Relief Upset Stomach And Nausea ReliefTRISODIUM CITRATE DIHYDRATE 230 mg/1 · Tablet, Chewable · WALGREENS CO.
NDC 0363-1834Label

Nigeria (NAFDAC)

NAFDACAlben ORS_ A11-0033NAFDACVadilyn Syrup 04-4148NAFDACVadilix Syrup_ 04-4113NAFDACCoughcare+ Syrup A11-100600NAFDACUgolab Baby Cough 04-4504NAFDACNalis Cough Syrup A11-100036NAFDACKofmed Expectorant A4-8980NAFDACExokuf Cough Syrup A11-100627NAFDACD-Koff Expectorant 04-2751NAFDACChildren`s Tuxil-N A4-5896NAFDACExiplon Expectorant 04-4252NAFDACEmzolyn Expectorant 04-0266

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti InoU.S. FDA Class II
3 Aug 2026 · Shoolin Pharma Chem LLP · OngoingCGMP Deviations:Noted during FDA inspection
SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti InoU.S. FDA Class II
3 Aug 2026 · Shoolin Pharma Chem LLP · OngoingCGMP Deviations:Noted during FDA inspection
Sildenafil Citrate USP for prescription compounding, packaged in a) 5g (NDC 58597-8088-2);b) 25g (NDC 58597-8088-4); c) 50g (NDC 58597-8088-5); d) 100g (NDC 58597-8088-6); e) 500g U.S. FDA Class II
9 Feb 2018 · American Pharmaceutical Ingredients LLC · TerminatedCGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Sildenafil Citrate active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4U.S. FDA Class II
14 Nov 2014 · Attix Pharmaceuticals · TerminatedPenicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they were repackaged in a facility with penicillin products without adequate separation which could introduce the poten

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Sodium citrate

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

Questions about Sodium citrate

What is Sodium citrate used for?

Sildenafil tablets are indicated for the treatment of erectile dysfunction. Sildenafil is a phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED) (From the official U.S. FDA label.)

How do I take Sodium citrate?

Follow your prescription or the leaflet in your pack. The official label says: For most patients, the recommended dose is 50 mg taken, as needed, approximately 1 hour before sexual activity. However, sildenafil tablets may be taken anywhere from 30 minutes to 4 hours before sexual activity ( 2.1 ) Based on effectiveness and toleration, may increase to a maximum of 100 mg or decrease to 25 mg ( 2.1 ) Maximum recommended dosing frequency is once per day ( 2…

Do I need a prescription for Sodium citrate?

Usually yes. Sodium citrate is a prescription medicine in most countries. Rules differ by country.

What brands contain Sodium citrate?

Sodium citrate is sold under names such as Cytra 2, Cytra-3, Oracit, Regiocit, Emetrol Chewables, Emetrol Powder, Bss Ophthalmic Solution, Sildenafil Citrate. Brand names differ between countries.

How can I check that my Sodium citrate is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.