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Dexbrompheniramine Maleate

Generic Name
Dexbrompheniramine Maleate

Overview

No overview information available.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
ACTIPHARMA, LLC
63102-402
ORAL
1 mg in 1 1
8/18/2025
Poly Pharmaceuticals, Inc.
50991-865
ORAL
2 mg in 1 1
4/28/2025

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
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
DRIXORAL DAY/NIGHT - SRT/TABS
schering-plough canada inc
02154285
Tablet (Extended-Release) ,  Tablet - Oral
2 MG
9/19/1996
DRIXTAB TAB
schering-plough canada inc
00411892
Tablet - Oral
2 MG
12/31/1980
DRIXORAL SYRUP
schering-plough canada inc
02175576
Syrup - Oral
1.5 MG / 5 ML
12/31/1996
CORICIDIN D NASAL AND SINUS CONGESTION TABLETS
schering-plough healthcare products canada, a division of schering canada inc.
02244653
Tablet (Extended-Release) - Oral
6 MG
N/A
CORICIDIN 'D' NASAL AND SINUS CONGESTION
schering-plough healthcare products canada, a division of schering canada inc.
02244303
Tablet (Extended-Release) - Oral
6 MG
N/A
DRIXORAL COLD & SINUS
bayer inc consumer care
00298433
Tablet (Extended-Release) - Oral
6 MG
12/31/1974

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.

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