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Drug ReportsMethscopolamine
Methscopolamine
Methscopolamine (methscopolamine) is a small molecule pharmaceutical. Methscopolamine was first approved as Pamine on 1982-01-01. It is used to treat peptic ulcer in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
digestive system diseasesD004066
Trade Name
FDA
EMA
Methscopolamine (discontinued: Methscopolamine, Pamine)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Methscopolamine bromide
Tradename
Company
Number
Date
Products
PAMINEFougera PharmaceuticalsN-008848 DISCN1982-01-01
1 products
PAMINE FORTEFougera PharmaceuticalsN-008848 DISCN2003-03-25
1 products
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Labels
FDA
EMA
Brand Name
Status
Last Update
methscopolamine bromideANDA2024-11-11
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
peptic ulcerHP_0004398D010437K27
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
No data
Drug
General
Drug common nameMethscopolamine
INN
Description
Scopolamine methobromide is a quaternary ammonium salt resulting from the reaction of the amino group of scopolamine with methyl bromide. It has a role as a muscarinic antagonist, an antiemetic, an antispasmodic drug and a parasympatholytic. It is a quaternary ammonium salt and a bromide salt. It is functionally related to a scopolamine.
Classification
Small molecule
Drug class
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Structure (InChI/SMILES or Protein Sequence)
C[N+]1(C)[C@H]2C[C@H](OC(=O)[C@H](CO)c3ccccc3)C[C@H]1[C@H]1O[C@@H]21
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL1201268
ChEBI ID
PubChem CID5459110
DrugBankDB00747
UNII ID
Target
No data
Variants
No data
Financial
Revenue by drug
$
£
No data
Estimated US medical usage
Methscopolamine
+
Chlorpheniramine
Total medical expenditures per year (USD, in millions)
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Methscopolamine
Total medical expenditures per year (USD, in millions)
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Methscopolamine
+
Pseudoephedrine
Total medical expenditures per year (USD, in millions)
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Tabular view
Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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