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Cogentin (benzatropine)

FDA-approved active Under review Quality 45/100

Cogentin (generic name: benzatropine) is a Anticholinergic drug. It is currently FDA-approved (first approved 1954) for Arteriosclerotic Parkinsonism, Extrapyramidal disease, Parkinson's disease.

Benztropine is a small molecule medication used to treat movement disorders such as parkinsonism and dystonia, as well as extrapyramidal side effects of antipsychotics. It is taken by mouth or by injection into a vein or muscle and works as a centrally acting anticholinergic and antihistamine.

At a glance

Generic namebenzatropine
Drug classAnticholinergic
TargetMuscarinic acetylcholine receptor M1
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1954

Approved indications

Common side effects

No common side effects on file.

Drug interactions

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
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Cogentin

What is Cogentin?

Cogentin (benzatropine) is a Anticholinergic drug, indicated for Arteriosclerotic Parkinsonism, Extrapyramidal disease, Parkinson's disease.

What is Cogentin used for?

Cogentin is indicated for Arteriosclerotic Parkinsonism, Extrapyramidal disease, Parkinson's disease, Parkinsonism, Postencephalitic parkinsonism.

What is the generic name of Cogentin?

benzatropine is the generic (nonproprietary) name of Cogentin.

What drug class is Cogentin in?

Cogentin belongs to the Anticholinergic class. See all Anticholinergic drugs at /class/anticholinergic.

When was Cogentin approved?

Cogentin was first approved on 1954.

What development phase is Cogentin in?

Cogentin is FDA-approved (marketed).

What does Cogentin target?

Cogentin targets Muscarinic acetylcholine receptor M1 and is a Anticholinergic.

Related

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