MedPath

Methscopolamine bromide

Generic Name
Methscopolamine bromide
Brand Names
Pamine
Drug Type
Small Molecule
Chemical Formula
C18H24BrNO4
CAS Number
155-41-9
Unique Ingredient Identifier
RTN51LK7WL

Overview

A muscarinic antagonist used to study binding characteristics of muscarinic cholinergic receptors.

Indication

Used as adjunctive therapy for the treatment of peptic ulcer. Also used to treat nausea and vomiting due to motion sickness.

Associated Conditions

  • Peptic Ulcer

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
BAYSHORE PHARMACEUTICALS LLC
76385-101
ORAL
5 mg in 1 1
4/11/2019
BAYSHORE PHARMACEUTICALS LLC
76385-100
ORAL
2.5 mg in 1 1
4/11/2019
Breckenridge Pharmaceutical, Inc.
51991-192
ORAL
5 mg in 1 1
1/10/2024
Aarkish Pharmaceuticals NJ Inc.
81005-127
ORAL
2.5 mg in 1 1
2/26/2024
PD-Rx Pharmaceuticals, Inc.
43063-740
ORAL
2.5 mg in 1 1
9/27/2023
PD-Rx Pharmaceuticals, Inc.
43063-741
ORAL
5 mg in 1 1
9/27/2023
Breckenridge Pharmaceutical, Inc.
51991-191
ORAL
2.5 mg in 1 1
1/10/2024
PharmaDerm a division of Fougera Pharmaceuticals Inc.
10337-062
ORAL
5 mg in 1 1
8/9/2012
AACE Pharmaceuticals, Inc.
71406-127
ORAL
5 mg in 1 1
2/5/2024
AACE Pharmaceuticals, Inc.
71406-126
ORAL
2.5 mg in 1 1
2/5/2024

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
U-METAMINE TAB 1MG
N/A
synco (h.k.) limited
N/A
N/A
3/13/1990
SCOPOLAMINE SYRUP 1MG/5ML
N/A
N/A
N/A
6/5/1987
HYOSCINE METHOBROMIDE SYR 1MG/5ML
N/A
N/A
N/A
1/24/1992

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.