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Ropivacaine 0.75% Injectable Solution

Paola M Zamora Munoz · FDA-approved active Small molecule ✓ Verified May 2026 Quality 5/100

Ropivacaine 0.75% Injectable Solution is a Small molecule drug developed by Paola M Zamora Munoz. It is currently FDA-approved. Also known as: parecoxib 40mg, ROPIN 0.75%, Alone, Ropivacaine.

Ropivacaine 0.75% Injectable Solution is a small molecule used for pain management, including postoperative pain, and has been studied in various clinical trials for its effectiveness in conditions such as post-thoracotomy pain and pain associated with neurosurgery, unplanned caesarean section, anorectal surgery, and other procedures. It is administered through methods such as erector spinae plane block, intercostal nerve block, and scalp blocks.

At a glance

Generic nameRopivacaine 0.75% Injectable Solution
Also known asparecoxib 40mg, ROPIN 0.75%, Alone, Ropivacaine
SponsorPaola M Zamora Munoz
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Ropivacaine 0.75% Injectable Solution

What is Ropivacaine 0.75% Injectable Solution?

Ropivacaine 0.75% Injectable Solution is a Small molecule drug developed by Paola M Zamora Munoz.

Who makes Ropivacaine 0.75% Injectable Solution?

Ropivacaine 0.75% Injectable Solution is developed and marketed by Paola M Zamora Munoz (see full Paola M Zamora Munoz pipeline at /company/paola-m-zamora-munoz).

Is Ropivacaine 0.75% Injectable Solution also known as anything else?

Ropivacaine 0.75% Injectable Solution is also known as parecoxib 40mg, ROPIN 0.75%, Alone, Ropivacaine.

What development phase is Ropivacaine 0.75% Injectable Solution in?

Ropivacaine 0.75% Injectable Solution is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing