bucladin-s
Bucladin-S (Buclizine Hydrochloride) is a medication used to treat Nausea, Vertigo, Vomiting.
Buclizine Hydrochloride · by Stuart Pharms
Key facts
- Active ingredient
- Buclizine Hydrochloride
- Form
- Tablet
- Strength
- Buclizine Hydrochloride 50MG
- Type
- Prescription (Rx)
- Brand or generic
- Brand-name
- Manufacturer
- Stuart Pharms
- FDA application
- NDA010911
- 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
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Frequently asked questions
- What does Bucladin-S treat?
- Bucladin-S (Buclizine Hydrochloride) may be used to treat nausea, vertigo, vomiting, 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 Bucladin-S?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Bucladin-S. 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 Bucladin-S?
- Bucladin-S is marketed by Stuart Pharms. You can see Stuart Pharms's full profile, rating, and other products on pharmaranks.
- Is Bucladin-S a brand-name or generic drug?
- Bucladin-S is a brand-name product with the active ingredient Buclizine Hydrochloride.
- Is Bucladin-S available over the counter?
- No. Bucladin-S 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 Bucladin-S come in?
- Bucladin-S is currently marketed as tablet, per the FDA's National Drug Code Directory.
- Is Bucladin-S FDA-registered?
- Bucladin-S is on record with the U.S. FDA under application number NDA010911. 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 BUCLIZINE HYDROCHLORIDE
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 65 reports naming BUCLIZINE HYDROCHLORIDE — the active ingredient in Bucladin-S, and the FDA flagged 94% 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:
- migraine9 reports
- hydronephrosis8 reports
- insomnia7 reports
- neuropathy peripheral7 reports
- sleep disorder7 reports
- disturbance in attention6 reports
- libido decreased6 reports
- nausea6 reports
Read these as a signal, not a rate. A report does not mean BUCLIZINE 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 25, 2026.
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