Milnacipran
Milnacipran is an SNRI (a type of medication that affects serotonin and norepinephrine in the brain) used to manage fibromyalgia in adults.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 6 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Milnacipran (Savella) is an SNRI, a drug that boosts two brain messengers, serotonin and norepinephrine, to dampen pain signals; it is one of a few medicines approved for fibromyalgia in adults, on the market since about 2009 and available as a generic. Nausea is the side effect most people notice early on, along with headache, constipation, sweating and a faster heartbeat. It is not approved for depression but carries a boxed warning about suicidal thoughts in young people, so watch for new mood changes, especially in the first weeks. It also raises blood pressure and heart rate, so get yours checked before starting and regularly after.
Clinical pearls
- Take each dose with a meal, since food often softens the nausea that is common in the first weeks.
- Tell every prescriber you take it, since tramadol, triptans, other antidepressants and St. John's Wort can trigger serotonin syndrome.
- Never stop it suddenly, even if it seems not to be working; your prescriber will taper it to avoid withdrawal symptoms.
- Regular ibuprofen, naproxen or aspirin use adds to its bleeding risk, so report unusual bruising or bleeding.
⚠️ FDA Boxed Warning — the FDA’s strongest safety alert ▾
Important warning about suicidal thoughts: Milnacipran belongs to a class of drugs similar to antidepressants. Studies show that antidepressants can increase the risk of suicidal thinking and behavior in children, teenagers, and young adults (especially those under 25) when used for depression or other psychiatric conditions. Closely watch anyone starting milnacipran — especially young adults — for new or worsening thoughts of suicide, unusual mood changes, agitation, or behavioral changes, and contact the prescriber right away if these occur. This risk is most important during the first few weeks of treatment or after a dose change. Families and caregivers should be involved in monitoring. Note: milnacipran is not approved to treat depression, and it is not approved for anyone under 18.
Patient information guide A plain-language walkthrough of Milnacipran, written from its FDA label.
What Milnacipran is used for
▾
Milnacipran is an SNRI used to manage fibromyalgia in adults.
- Milnacipran Hydrochloride tablets are indicated for the management of fibromyalgia
- Savella (milnacipran) tablets are indicated for the management of fibromyalgia
- Milnacipran is not approved to treat major depressive disorder or any other psychiatric condition
- Milnacipran is not approved for use in patients under 18 years of age
How Milnacipran works
▾
Milnacipran is a serotonin-norepinephrine reuptake inhibitor (SNRI). It works by preventing the brain from reabsorbing two neurotransmitters — norepinephrine and serotonin — leaving more of them active in the nervous system. It preferentially blocks norepinephrine reuptake with about three times the potency of serotonin reuptake. Although the exact reason this helps fibromyalgia pain is not fully understood, it is thought to involve the brain's ability to dampen pain signals. Milnacipran does not significantly bind to a wide range of other brain receptors (such as those for histamine, dopamine, or acetylcholine), which distinguishes it from older medications and may limit certain side effects.
Milnacipran dosage
▾
Milnacipran tablets are taken by mouth twice a day. They can be taken with or without food, though food may help with stomach upset. The dose is started low on day one and gradually stepped up over the course of about a week to improve tolerability — your prescriber will give you a specific schedule to follow.
- Do not stop taking milnacipran suddenly; the dose should be tapered gradually
- If you have significant kidney problems, your dose may need to be adjusted or the medication may not be appropriate for you
- Always follow your prescriber's exact instructions — do not adjust your dose on your own
Dosing details from the FDA-approved label
From the Milnacipran prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- General dosing (recommended dosing)
- Recommended dose is 100 mg/day (50 mg twice daily), given orally in two divided doses per day with or without food
- Titration based on efficacy and tolerability: Day 1: 12.5 mg once
- Days 2 to 3: 25 mg/day (12.5 mg twice daily)
- Days 4 to 7: 50 mg/day (25 mg twice daily)
- After Day 7: 100 mg/day (50 mg twice daily)
- Based on individual patient response, may
- Maximum: Doses above 200 mg/day have not been studied
- Taking with food may improve tolerability; taper and do not abruptly discontinue after extended use
- Patients with severe renal impairment (estimated creatinine clearance of 5 to 29 mL/min)
- Reduce the maintenance dose by 50% to 50 mg/day (25 mg twice daily)
- Based on individual patient response, may be increased to 100 mg/day (50 mg twice daily)
- Not recommended for end-stage renal disease; no adjustment for mild renal impairment; use caution in moderate renal impairment
- Patients with hepatic impairment
- No dosage adjustment is necessary
- Exercise caution in patients with severe hepatic impairment
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION Milnacipran hydrochloride tablets are given orally with or without food. Taking milnacipran hydrochloride tablets with food may improve the tolerability of the drug. • Administer milnacipran hydrochloride tablets in two divided doses per day (2.1) . • Based on efficacy and tolerability, dosing may be titrated according to the following schedule (2.1) : Day 1: 12.5 mg once Days 2 to 3: 25 mg/day (12.5 mg twice daily) Days 4 to 7: 50 mg/day (25 mg twice daily) After Day 7: 100 mg/day (50 mg twice daily) • Recommended dose is 100 mg/day (2.1) . • May be increased to 200 mg/day based on individual patient response (2.1) . • Adjust dose in patients with severe renal impairment (2.2) . 2.1 Recommended Dosing The recommended dose of milnacipran hydrochloride tablet is 100 mg/day (50 mg twice daily). Based on efficacy and tolerability dosing may be titrated according to the following schedule: Day 1: 12.5 mg once Days 2 to 3: 25 mg/day (12.5 mg twice daily) Days 4 to 7: 50 mg/day (25 mg twice daily) After Day 7: 100 mg/day (50 mg twice daily) Based on individual patient response, the dose may be increased to 200 mg/day (100 mg twice daily). Doses above 200 mg/day have not been studied. Taper milnacipran hydrochloride tablets and do not abruptly discontinue after extended use [see Dosage and Administration (2.4) , Warnings and Precautions (5.7) ]. 2.2 Patients with Renal Insufficiency No dosage adjustment is necessary in patients with mild renal impairment. Use milnacipran hydrochloride tablets with caution in patients with moderate renal impairment. For patients with severe renal impairment (indicated by an estimated creatinine clearance of 5 to 29 mL/min), reduce the maintenance dose by 50% to 50 mg/day (25 mg twice daily). Based on individual patient response, the dose may be increased to 100 mg/day (50 mg twice daily). Milnacipran hydrochloride tablets are not recommended for patients with end-stage renal disease. 2.3 Patients with Hepatic Insufficiency No dosage adjustment is necessary for patients with hepatic impairment. As with any drug, exercise caution in patients with severe hepatic impairment.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Milnacipran side effects
▾
The most common side effects reported in clinical trials include:
Common side effects
- Nausea
- Headache
- Constipation
- Dizziness
- Insomnia (trouble sleeping)
- Hot flushes and excessive sweating
- Palpitations (noticeable heartbeat) or faster heart rate
- High blood pressure
- Dry mouth
- Vomiting
When to get medical help
- Seek emergency help if you notice signs of serotonin syndrome: agitation, hallucinations, rapid heartbeat, fever, severe muscle twitching, or loss of coordination
- Call your doctor right away if your blood pressure rises significantly or you develop chest pain
- Get help immediately if you have thoughts of suicide or self-harm, or notice unusual changes in mood or behavior
- Contact your doctor if you experience signs of liver problems: yellowing of the skin or eyes, dark urine, severe stomach pain
- Tell your doctor if you have unusual bleeding or bruising, especially if you also take aspirin, NSAIDs, or blood thinners
- Seek care for seizures (convulsions) — cases have been reported with milnacipran
- Call your doctor if you develop difficulty urinating, especially if you are male with a history of urinary problems
More serious reactions — including serotonin syndrome, significant blood pressure increases, liver problems, abnormal bleeding, and seizures — have been reported. Contact your doctor or seek emergency care right away if any of these occur.
Milnacipran warnings and precautions
▾
- Suicidal thinking: Like other SNRI-class drugs, milnacipran is associated with an increased risk of suicidal thoughts in children, adolescents, and young adults. Monitor closely, especially early in treatment or after dose changes. Milnacipran is not approved for anyone under 18.
- Serotonin syndrome: A potentially life-threatening condition can occur if milnacipran is combined with MAOIs or other serotonergic drugs. Symptoms include agitation, hallucinations, rapid heartbeat, fever, muscle twitching, and loss of coordination. Seek emergency help immediately.
- High blood pressure and heart rate: Milnacipran can meaningfully raise blood pressure and heart rate. Blood pressure should be checked before starting and monitored regularly during treatment.
- Bleeding risk: Milnacipran affects how platelets work, increasing bleeding risk — especially when combined with NSAIDs, aspirin, or blood thinners.
- Liver concerns: Milnacipran can raise liver enzymes. Avoid heavy alcohol use or use in people with chronic liver disease.
- Discontinuation symptoms: Do not stop milnacipran abruptly. A gradual taper is needed to avoid withdrawal-like symptoms.
- Seizures: Cases have been reported; use with caution if you have a seizure history.
- Urinary problems in men: Men with a history of obstructive urinary conditions may experience higher rates of urinary side effects.
Milnacipran interactions
▾
Milnacipran has few pharmacokinetic (blood level) drug interactions because it is mostly excreted unchanged and does not significantly affect liver enzymes. However, it does have important pharmacodynamic (how it acts) interactions:
- MAOIs (e.g., phenelzine, tranylcypromine, linezolid, IV methylene blue) — dangerous serotonin syndrome risk; strictly contraindicated; a washout period is required before switching
- Other serotonergic drugs (SSRIs, SNRIs, triptans, tricyclic antidepressants, tramadol, fentanyl, meperidine, methadone, lithium, tryptophan, buspirone, amphetamines, St. John's Wort) — increased serotonin syndrome risk
- Epinephrine and norepinephrine — may cause dangerous blood pressure spikes or heart rhythm problems
- IV digoxin — may worsen heart-related side effects including low blood pressure and rapid heart rate; avoid this combination
- Clonidine — milnacipran may reduce clonidine's blood-pressure-lowering effect
- NSAIDs, aspirin, warfarin, and other antiplatelet or anticoagulant drugs — increased risk of bleeding
- Clomipramine — switching from clomipramine without a washout period may cause low blood pressure and euphoria
Interactions listed in the FDA-approved label
From the Milnacipran prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Monoamine oxidase inhibitors (MAOIs) intended to treat psychiatric disorders: Concomitant use of SSRIs and SNRIs, including milnacipran, with MAOIs increases the risk of serotonin syndrome; use with an MAOI or within 5 days of stopping milnacipran, or within 14 days of stopping an MAOI, is contraindicated. Allow at least 14 days after stopping an MAOI before starting milnacipran, and at least 5 days after stopping milnacipran before starting an MAOI.
- Linezolid or intravenous methylene blue (MAOIs): Increased risk of serotonin syndrome. Do not initiate milnacipran in a patient being treated with them; if treatment is necessary in a patient taking milnacipran, discontinue milnacipran before initiating the MAOI.
- Other serotonergic drugs (other SNRIs, SSRIs, triptans, tricyclic antidepressants, opioids, lithium, tryptophan, buspirone, amphetamines, St. John's Wort): Serotonin syndrome can occur with milnacipran and other serotonergic drugs. Advise patients of the signs and symptoms of serotonin syndrome and to seek medical care immediately if they occur.
- Triptans: There have been rare postmarketing reports of serotonin syndrome with use of an SSRI and a triptan. If concomitant treatment is clinically warranted, careful observation is advised, particularly during treatment initiation and dose increases.
- Epinephrine and norepinephrine (catecholamines): Concomitant use may be associated with paroxysmal hypertension and possible arrhythmia because milnacipran inhibits norepinephrine reuptake.
- Other CNS-active drugs (including clomipramine): In a drug-drug interaction study, an increase in euphoria and postural hypotension was observed in patients who switched from clomipramine to milnacipran. Use caution when taken in combination with other centrally acting drugs.
- Digoxin: May be associated with potentiation of adverse hemodynamic effects; postural hypotension and tachycardia were reported with intravenous digoxin (1 mg). Avoid co-administration of milnacipran and intravenous digoxin.
- Clonidine: Co-administration may inhibit clonidine's anti-hypertensive effect because milnacipran inhibits norepinephrine reuptake.
- Antiplatelet or anticoagulant drugs (e.g., NSAIDs, aspirin, warfarin): Concomitant use may potentiate the risk of bleeding. Closely monitor for bleeding when milnacipran is initiated or discontinued.
Read the label’s full interactions text
7 DRUG INTERACTIONS Milnacipran undergoes minimal CYP450 related metabolism, with the majority of the dose excreted unchanged in urine (55%) and has a low binding to plasma proteins (13%). In vitro and in vivo studies showed that milnacipran hydrochloride is unlikely to be involved in clinically significant pharmacokinetic drug interactions [see Pharmacokinetics in Special Populations ( 12.3 )] . • Milnacipran hydrochloride is unlikely to be involved in clinically significant pharmacokinetic drug interactions ( 7 ). • Pharmacodynamic interactions of milnacipran hydrochloride with other drugs can occur ( 7 ). 7.1 Monoamine Oxidase Inhibitors (MAOIs) The concomitant use of SSRIs and SNRIs, including milnacipran hydrochloride, with MAOIs increases the risk of serotonin syndrome. The use of MAOIs intended to treat psychiatric disorders with milnacipran hydrochloride or within 5 days of stopping treatment with milnacipran hydrochloride is contraindicated. The use of milnacipran hydrochloride within 14 days of stopping an MAOI intended to treat psychiatric disorders is also contraindicated. In addition, do not initiate milnacipran hydrochloride in a patient who is being treated with MAOIs such as linezolid or intravenous methylene blue. No reports involved the administration of methylene blue by other routes (such as oral tablets or local tissue injection). If it is necessary to initiate treatment with a MAOI such as linezolid or intravenous methylene blue in a patient taking milnacipran hydrochloride, discontinue milnacipran hydrochloride before initiating treatment with the MAOI [see Dosage and Administration ( 2.5 , 2.6 ), Contraindications ( 4 ), Drug Interactions ( 7.1 )] . 7.2 Serotonergic Drugs Serotonin syndrome can occur with use of milnacipran hydrochloride and other serotonergic drugs (other SNRIs, SSRIs, triptans, tricyclic antidepressants, opioids, lithium, tryptophan, buspirone, amphetamines, and St.
Excerpted — the section continues on the label. Read the full Drug Interactions section on DailyMed →
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Milnacipran
▾
- Tell your doctor about all medications you take, especially MAOIs, antidepressants, triptans, blood thinners, and pain relievers like NSAIDs
- Inform your doctor if you have kidney disease — milnacipran is primarily cleared by the kidneys, and those with severe impairment need a lower dose; it is not recommended for end-stage kidney disease
- Tell your doctor if you have liver disease or drink alcohol heavily — caution is needed, especially with severe liver impairment
- Disclose any history of high blood pressure or heart problems — milnacipran can raise blood pressure and heart rate
- Tell your doctor if you have a history of seizures
- Men with a history of urinary obstruction or difficulty urinating should discuss this with their doctor before starting
- If you are pregnant or planning to become pregnant: using milnacipran late in pregnancy may cause complications in the newborn and may increase the risk of postpartum hemorrhage — discuss the risks and benefits with your doctor
- If you are breastfeeding: milnacipran passes into breast milk; monitor the infant for agitation, irritability, poor feeding, and poor weight gain
- Milnacipran is not approved for patients under 18
- Older adults should have kidney function assessed before starting, since milnacipran levels may be higher due to age-related decline in kidney function
Milnacipran overdose
▾
Taking too much milnacipran can cause increased blood pressure, changes in consciousness (from drowsiness to coma), confusion, dizziness, and in serious cases, cardiac and respiratory problems. There is no specific antidote. If an overdose is suspected, call Poison Control or go to the nearest emergency room immediately — do not try to induce vomiting.
What Milnacipran does in the body
▾
Milnacipran can raise blood pressure and heart rate, effects that have been measured in clinical studies. In studies of fibromyalgia patients, a meaningful proportion of those taking milnacipran developed blood pressure readings in the high range compared with those taking placebo, making blood pressure monitoring an important part of treatment. At doses far above the therapeutic range, milnacipran produced a small increase in the QTcF interval (a measure of heart electrical activity), but this was not considered clinically significant.
How your body processes Milnacipran
▾
Milnacipran is well absorbed when taken by mouth — about 85–90% of a dose reaches the bloodstream — and food does not affect absorption. It reaches peak blood levels within 2 to 4 hours and has a half-life (the time for the body to eliminate half the drug) of about 6 to 8 hours, so steady levels are reached within about 36 to 48 hours of regular dosing. Unlike many medications, milnacipran is mostly excreted unchanged through the kidneys (about 55% of the dose), which means kidney function has a significant impact on how the drug behaves in the body. It has very low binding to blood proteins (13%) and does not meaningfully inhibit or induce the liver enzymes (CYP450) responsible for metabolizing many other drugs, which limits most pharmacokinetic drug interactions.
How to store Milnacipran
▾
Store at 25°C (77°F); excursions permitted between 15°C and 30°C (between 59°F and 86°F) .
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Milnacipran: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Milnacipran — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly is milnacipran used for — is it an antidepressant?
▾
Nausea seems really common with this medication — is there anything I can do about it?
▾
I heard this can affect my blood pressure. Should I be monitoring it at home?
▾
Can I just stop taking milnacipran if I decide it's not working for me?
▾
Are there medications I absolutely cannot take with milnacipran?
▾
Is it safe to take milnacipran during pregnancy or while breastfeeding?
▾
Is Milnacipran available over the counter?
▾
When was Milnacipran first available?
▾
Who makes Milnacipran?
▾
Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Milnacipran on HelloPharmacist
Milnacipran forms and strengths (how it comes)
Milnacipran is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Need a version that does not list lactose, a gluten source, a dye or gelatin? Inactive ingredients differ by manufacturer: see Milnacipran inactive ingredients by manufacturer.
Tablet
How this form is used
- Milnacipran Hydrochloride tablets are indicated for the management of fibromyalgia in adults
- Savella tablets are indicated for the management of fibromyalgia in adults
- Milnacipran Hydrochloride and Savella tablets are taken by mouth twice daily
- Milnacipran Hydrochloride and Savella tablets can be taken with or without food; taking with food may improve tolerability
- Savella and Milnacipran Hydrochloride tablets are started at a low dose and gradually increased over the first week or more — follow your prescriber's titration schedule
- Do not stop Savella or Milnacipran Hydrochloride tablets abruptly; the dose should be tapered gradually under your prescriber's guidance
Milnacipran on the U.S. market: products, makers and brands
How Milnacipran appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
7 companies list 27 Milnacipran product records with the FDA, mostly as tablet; the earliest marketing or approval year on record is 2009. Brand names on the directory include Savella; the rest are generics.
Also listed with the FDA, not a patient dose form: Kit (6) · Powder (5) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
How widely Milnacipran is used (Medicaid data)
A general measure of how commonly Milnacipran is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Milnacipran is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Milnacipran prescribed? Of the 1,601 medications we measure, Milnacipran ranks #749 by Medicaid prescriptions — more than 53% of them.
Utilization by Milnacipran product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
milnacipran hydrochloride 50 MG Oral Tablet Most dispensed
Summed across the 1 of 12 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 833144
milnacipran hydrochloride 100 MG Oral Tablet
Summed across the 1 of 10 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 833135
milnacipran hydrochloride 25 MG Oral Tablet
Summed across the 1 of 10 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 833147
milnacipran hydrochloride 12.5 MG Oral Tablet
Summed across the 1 of 9 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 833141
Other Milnacipran products — combination packs and listings not yet matched to a specific clinical product (kept visible so every prescription is accounted for)
Summed across the 1 of 7 listed NDC products with Medicaid activity.
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Milnacipran, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 5 of 48 listed Milnacipran NDCs with Medicaid activity.
Compare Milnacipran products
A representative set of FDA-listed product records for Milnacipran — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Tablet | ||||
| 12.5 mg | Oral | Allergan, Inc. | NDA | View NDC → |
| 25 mg | Oral | Allergan, Inc. | NDA | View NDC → |
| 50 mg | Oral | Allergan, Inc. | NDA | View NDC → |
| 100 mg | Oral | Allergan, Inc. | NDA | View NDC → |
| 12.5 mg | Oral | Amneal Pharmaceuticals LLC | ANDA | View NDC → |
| 25 mg | Oral | Amneal Pharmaceuticals LLC | ANDA | View NDC → |
| 50 mg | Oral | Amneal Pharmaceuticals LLC | ANDA | View NDC → |
| 100 mg | Oral | Amneal Pharmaceuticals LLC | ANDA | View NDC → |
| 12.5 mg | Oral | Breckenridge Pharmaceutical, Inc. | ANDA | View NDC → |
| 25 mg | Oral | Breckenridge Pharmaceutical, Inc. | ANDA | View NDC → |
| 50 mg | Oral | Breckenridge Pharmaceutical, Inc. | ANDA | View NDC → |
| 100 mg | Oral | Breckenridge Pharmaceutical, Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 25 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 50 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 100 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 50 mg | Oral | Cardinal Health 107, LLC | NDA | View NDC → |
| 12.5 mg | Oral | Glenmark Pharmaceuticals Inc., USA | NDA AUTHORIZED GENERIC | View NDC → |
| 25 mg | Oral | Glenmark Pharmaceuticals Inc., USA | NDA AUTHORIZED GENERIC | View NDC → |
| 50 mg | Oral | Glenmark Pharmaceuticals Inc., USA | NDA AUTHORIZED GENERIC | View NDC → |
| 100 mg | Oral | Glenmark Pharmaceuticals Inc., USA | NDA AUTHORIZED GENERIC | View NDC → |
| 12.5 mg | Oral | Macleods Pharmaceuticals Limited | ANDA | View NDC → |
| 25 mg | Oral | Macleods Pharmaceuticals Limited | ANDA | View NDC → |
| 50 mg | Oral | Macleods Pharmaceuticals Limited | ANDA | View NDC → |
| 100 mg | Oral | Macleods Pharmaceuticals Limited | ANDA | View NDC → |
| 💊Kits | ||||
| — | Oral | Allergan, Inc. | NDA | View NDC → |
| — | — | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
Showing 27 of 27 products — FDA National Drug Code Directory. See every product, package size and price: browse all 27 Milnacipran NDCs →
Milnacipran side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Milnacipran — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Milnacipran in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Milnacipran FDA approval history
How Milnacipran went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Milnacipran recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Milnacipran recalls since July 2021.
✅No Milnacipran recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 588250 1 dose form · 4 strengths
-
Dose form (SCDF) Oral Tablet RxCUI 833134In current FDA listingsClinical drug / strength (SCD) hydrochloride 100 MGRxCUI 833135hydrochloride 12.5 MGRxCUI 833141hydrochloride 25 MGRxCUI 833147hydrochloride 50 MGRxCUI 833144
Look up RxCUI 588250 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Milnacipran supply and shortage status
Whether Milnacipran is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
💵 What Milnacipran costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Tablet, Film Coated · Oral | 50 mg | $8.16 per tablet | NDC details & price history |
| Tablet, Film Coated · Oral | 100 mg | $8.15 per tablet | NDC details & price history |
| Tablet, Film Coated · Oral | 12.5 mg | $8.16 per tablet | NDC details & price history |
| Tablet, Film Coated · Oral | 25 mg | $8.16 per tablet | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Milnacipran brand names
Milnacipran is sold under one brand name in the FDA directory — Savella. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Milnacipran: manufacturers and labelers
7 companies list Milnacipran products with the FDA. By number of product records, the largest are Allergan, Inc., Camber Pharmaceuticals, Inc., Amneal Pharmaceuticals LLC. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Milnacipran drug class (RxNorm)
Milnacipran belongs to the Serotonin and Norepinephrine Reuptake Inhibitor class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
Sources for this Milnacipran page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Glenmark Pharmaceuticals Inc., USA is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →