dipivefrin hydrochloride
Dipivefrin Hydrochloride is a medication used to treat Open-Angle Glaucoma.
Generic · by Bausch and Lomb
Generic of Propine
Key facts
- Active ingredient
- Dipivefrin Hydrochloride
- Form
- Drops
- Strength
- Dipivefrin Hydrochloride 0.1%
- Type
- Prescription (Rx)
- Brand or generic
- Generic
- May treat
- open-angle glaucoma
- Manufacturer
- Bausch and Lomb
- FDA application
- ANDA074188
- Availability
- Discontinued (per FDA)
May treat (source: NIH RxClass)
Dosage forms
Drops
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 Dipivefrin Hydrochloride treat?
- Dipivefrin Hydrochloride (Dipivefrin Hydrochloride) may be used to treat open-angle glaucoma, 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 Dipivefrin Hydrochloride?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Dipivefrin Hydrochloride. To pay less, Dipivefrin Hydrochloride is already a generic — usually the lowest-cost version — so the main levers are comparing cash prices between pharmacies and using a pharmacy discount-card service. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
- Who makes Dipivefrin Hydrochloride?
- Dipivefrin Hydrochloride is marketed by Bausch and Lomb. You can see Bausch and Lomb's full profile, rating, and other products on pharmaranks.
- Is Dipivefrin Hydrochloride a brand-name or generic drug?
- Dipivefrin Hydrochloride is a generic medication; its active ingredient is Dipivefrin Hydrochloride. Generics contain the same active ingredient as the brand-name original and are usually lower cost.
- Is Dipivefrin Hydrochloride available over the counter?
- No. Dipivefrin Hydrochloride 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 Dipivefrin Hydrochloride come in?
- Dipivefrin Hydrochloride is currently marketed as drops, per the FDA's National Drug Code Directory.
- Is Dipivefrin Hydrochloride FDA-registered?
- Dipivefrin Hydrochloride is on record with the U.S. FDA under application number ANDA074188. 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 Dipivefrin Hydrochloride
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 9 reports naming Dipivefrin Hydrochloride, and the FDA flagged 78% 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:
- cardiomegaly2 reports
- confusional state2 reports
- amnesia1 reports
- arthropathy1 reports
- atherosclerosis1 reports
- c-reactive protein increased1 reports
- cardiac failure congestive1 reports
- cerebrovascular accident1 reports
Read these as a signal, not a rate. A report does not mean Dipivefrin 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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