MedPath

Magaldrate

Generic Name
Magaldrate
Drug Type
Small Molecule
Chemical Formula
Al5H33Mg10O40S2
CAS Number
74978-16-8
Unique Ingredient Identifier
6V88E24N5T

Overview

Magaldrate is an antacid drug used for the treatment of esophagitis, duodenal and gastric ulcers, and gastroesophageal reflux. Magaldrate has been discontinued in the US market.

Indication

用于缓解消化道溃疡、反流性食管炎、急慢性胃炎等酸相关性疾病的症状,如反酸、上腹痛、烧心、腹部不适、嗳气、腹胀等。

Associated Conditions

  • Bloating
  • Dyspepsia
  • Heartburn
  • Stress Ulcers

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

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
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
MYLANTA 2GO ANTACID DUAL ACTION tablet blister pack
14378
Medicine
A
9/20/1991

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
RIOPAN SUSPENSION 480MG/5ML
wyeth-ayerst canada inc.
02043580
Suspension - Oral
480 MG / 5 ML
12/31/1994
RIOPAN TAB 480MG
whitehall-robins inc.
01931059
Tablet - Oral
480 MG
12/31/1993
RIOPAN PLUS TABLETS
whitehall-robins inc.
01929461
Tablet - Oral
480 MG / TAB
12/31/1993
RIOPAN CHEWABLE TABLETS 480MG
wyeth-ayerst canada inc.
02043564
Tablet - Oral
480 MG
12/31/1994
RIOPAN PLUS SUSPENSION
whitehall-robins inc.
01929410
Suspension - Oral
96 MG / ML
12/31/1993
RIOPAN PLUS SUS
wyeth-ayerst canada inc.
02043572
Suspension - Oral
480 MG / 5 ML
12/31/1994
RIOPAN SUS 480MG/5ML
whitehall-robins inc.
01931067
Suspension - Oral
480 MG / 5 ML
12/31/1993

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
BEMOLAN 2000 mg GEL ORAL
Takeda Farmaceutica Espana S.A.
60765
GEL ORAL
Sin Receta
Commercialized
BEMOLAN 800 mg GEL ORAL
Takeda Farmaceutica Espana S.A.
57295
GEL ORAL
Sin Receta
Commercialized

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.

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