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Triprolidine Hydrochloride

Generic Name
Triprolidine Hydrochloride

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
STI Pharma LLC
54879-005
ORAL
1.25 mg in 5 mL
7/29/2015

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
SINIFED TAB
N/A
N/A
N/A
5/11/2012
UNI-FEDRA COMPOUND SYRUP
N/A
N/A
N/A
6/22/1990
UNI-FEDRA TABLET
N/A
N/A
N/A
5/2/2013
UNI-FEDRA DM SYRUP
N/A
N/A
N/A
4/23/1998
DOCTOR COUGH SYRUP
N/A
synco (h.k.) limited
N/A
N/A
3/11/1999
DUOFED TABLETS
N/A
N/A
N/A
3/25/2013

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