surmontil
Surmontil (Trimipramine Maleate) is a tricyclic antidepressant used to treat Depressive Disorder.
Trimipramine Maleate · by Teva Womens
Key facts
- Active ingredient
- Trimipramine Maleate
- Drug class
- Tricyclic Antidepressant
- Form
- Capsule
- Strength
- Trimipramine Maleate EQ 100MG Base **Federal Register Determination That Product was not Discontinued or Withdrawn for Safety or Effectiveness reasons** · Trimipramine Maleate EQ 25MG Base **Federal Register Determination That Product was not Discontinued or Withdrawn for Safety or Effectiveness reasons** · Trimipramine Maleate EQ 50MG Base **Federal Register Determination That Product was not Discontinued or Withdrawn for Safety or Effectiveness reasons**
- Type
- Prescription (Rx)
- Brand or generic
- Brand-name
- May treat
- depressive disorder
- Manufacturer
- Teva Womens
- FDA application
- NDA016792
- Availability
- Discontinued (per FDA)
Drug class
May treat (source: NIH RxClass)
See how Surmontil ranks — best-rated tricyclic antidepressant for:
Dosage forms
Capsule
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
Ways to save
Ask for the generic
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Request a 90-day supply
Bulk fills usually lower the per-dose price vs monthly refills.
Use copay cards
Manufacturer copay cards & patient-assistance programs — especially for brand drugs.
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Frequently asked questions
- What does Surmontil treat?
- Surmontil (Trimipramine Maleate) may be used to treat depressive disorder, based on NIH RxClass drug-classification data (conditions a drug may treat — not a verbatim copy of the FDA-approved label). This is general reference, not medical advice.
- Is there a coupon or discount for Surmontil?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Surmontil. To pay less, ask your prescriber or pharmacist whether a generic equivalent exists, check the manufacturer's copay/savings card and patient-assistance program, and compare a pharmacy discount card against your insurance copay. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
- Who makes Surmontil?
- Surmontil is marketed by Teva Womens. You can see Teva Womens's full profile, rating, and other products on pharmaranks.
- Is Surmontil a brand-name or generic drug?
- Surmontil is a brand-name product with the active ingredient Trimipramine Maleate.
- Is Surmontil available over the counter?
- No. Surmontil is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.
- What forms does Surmontil come in?
- Surmontil is currently marketed as capsule, per the FDA's National Drug Code Directory.
- What class of drug is Surmontil?
- Surmontil is classified as tricyclic antidepressant, per the FDA's Established Pharmacologic Class.
- Is Surmontil FDA-registered?
- Surmontil is on record with the U.S. FDA under application number NDA016792. You can verify this on its official FDA label.
Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
What people report to the FDA about TRIMIPRAMINE MALEATE
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 456 reports naming TRIMIPRAMINE MALEATE — the active ingredient in Surmontil, and the FDA flagged 93% 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:
- fatigue38 reports
- depression36 reports
- nausea27 reports
- fall25 reports
- vomiting25 reports
- coma23 reports
- dizziness23 reports
- diarrhoea19 reports
Read these as a signal, not a rate. A report does not mean TRIMIPRAMINE MALEATE 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.
Source: openFDA drug/event (FAERS), retrieved September 26, 2026.
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