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Proparacaine
Kainair, Ophthaine, Ophthetic, Paracaine (proparacaine) is a small molecule pharmaceutical. Proparacaine was first approved as Ophthetic on 1982-01-01.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Proparacaine hydrochloride
Tradename
Company
Number
Date
Products
OPHTHETICAllerganN-012583 DISCN1982-01-01
1 products, RLD
OPHTHAINEBristol Myers SquibbN-008883 DISCN1982-01-01
1 products, RLD
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Labels
FDA
EMA
Brand Name
Status
Last Update
alcaine ANDA2020-12-14
proparacaine hydrochlorideANDA2023-02-22
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
S: Sensory organ drugs
S01: Ophthalmologicals
S01H: Local anesthetics, ophthalmologic
S01HA: Local anesthetics
S01HA04: Proxymetacaine
HCPCS
No data
Clinical
Clinical Trials
2 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Urinary calculiD014545N20.911
Indications Phases 3
No data
Indications Phases 2
No data
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Overactive urinary bladderD053201EFO_1000781N32.8111
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common namePROPARACAINE
INNproxymetacaine
Description
Proparacaine is a benzoate ester.
Classification
Small molecule
Drug classlocal anesthetics
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CCCOc1ccc(C(=O)OCCN(CC)CC)cc1N
Identifiers
PDB
CAS-ID499-67-2
RxCUI34905
ChEMBL IDCHEMBL1196
ChEBI ID8485
PubChem CID4935
DrugBankDB00807
UNII IDB4OB0JHI1X (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 5,601 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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55 adverse events reported
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