lumenhance
Lumenhance (Manganese Chloride Tetrahydrate) is a medication supplied as a for solution.
Manganese Chloride Tetrahydrate · by Bracco
Key facts
- Active ingredient
- Manganese Chloride Tetrahydrate
- Strength
- Manganese Chloride Tetrahydrate 3.49MG/GM
- Type
- Prescription (Rx)
- Brand or generic
- Brand-name
- Manufacturer
- Bracco
- FDA application
- NDA020686
- Availability
- Discontinued (per FDA)
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
- Is there a coupon or discount for Lumenhance?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Lumenhance. 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 Lumenhance?
- Lumenhance is marketed by Bracco. You can see Bracco's full profile, rating, and other products on pharmaranks.
- Is Lumenhance a brand-name or generic drug?
- Lumenhance is a brand-name product with the active ingredient Manganese Chloride Tetrahydrate.
- Is Lumenhance available over the counter?
- No. Lumenhance 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.
- Is Lumenhance FDA-registered?
- Lumenhance is on record with the U.S. FDA under application number NDA020686. 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 MANGANESE CHLORIDE TETRAHYDRATE
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 1 reports naming MANGANESE CHLORIDE TETRAHYDRATE — the active ingredient in Lumenhance, and the FDA flagged 100% 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:
- blood pressure increased1 reports
- nasal congestion1 reports
Read these as a signal, not a rate. A report does not mean MANGANESE CHLORIDE TETRAHYDRATE 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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