ticlid
Ticlid (Ticlopidine Hydrochloride) is a medication used to treat Intracranial Embolism and Thrombosis.
Ticlopidine Hydrochloride · by Roche Palo
Available as a generic: Ticlopidine Hydrochloride
Key facts
- Active ingredient
- Ticlopidine Hydrochloride
- Form
- Tablet
- Strength
- Ticlopidine Hydrochloride 125MG · Ticlopidine Hydrochloride 250MG
- Type
- Prescription (Rx)
- Brand or generic
- Brand-name
- May treat
- intracranial embolism and thrombosis
- Manufacturer
- Roche Palo
- FDA application
- NDA019979
- Availability
- Discontinued (per FDA)
May treat (source: NIH RxClass)
Dosage forms
Tablet
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
Ways to save
Ask for the generic
Same active ingredient, far cheaper. Is there a generic? →
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.
Compare alternatives
A same-class option may cost less. See alternatives →
Frequently asked questions
- What does Ticlid treat?
- Ticlid (Ticlopidine Hydrochloride) may be used to treat intracranial embolism and thrombosis, 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 Ticlid?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Ticlid. 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 Ticlid?
- Ticlid is marketed by Roche Palo. You can see Roche Palo's full profile, rating, and other products on pharmaranks.
- Is Ticlid a brand-name or generic drug?
- Ticlid is a brand-name product with the active ingredient Ticlopidine Hydrochloride. Lower-cost generic equivalents containing Ticlopidine Hydrochloride are available — ask your pharmacist.
- Is Ticlid available over the counter?
- No. Ticlid 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 Ticlid come in?
- Ticlid is currently marketed as tablet, per the FDA's National Drug Code Directory.
- Is Ticlid FDA-registered?
- Ticlid is on record with the U.S. FDA under application number NDA019979. 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 TICLOPIDINE HYDROCHLORIDE
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 767 reports naming TICLOPIDINE HYDROCHLORIDE — the active ingredient in Ticlid, and the FDA flagged 98% 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:
- pyrexia35 reports
- anaemia32 reports
- asthenia28 reports
- diarrhoea28 reports
- malaise22 reports
- nausea22 reports
- fall20 reports
- vomiting20 reports
Read these as a signal, not a rate. A report does not mean TICLOPIDINE HYDROCHLORIDE 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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