Active ingredient
Triprolidine
5 finished FDA listings contain Triprolidine as their only active ingredient; 33 combination products also contain it.
FDA NDC Directory
- Ingredient names as written by FDA
- TRIPROLIDINE HYDROCHLORIDE
- Dosage forms
- Liquid, Syrup
- Routes
- Oral
- Manufacturers / labelers
- 3
- Strengths listed
- .938 mg/ml · 1.25 mg/2ml · 1.25 mg/ml · 2.5 mg/5ml
- Brand names in FDA listings
- Childrens Pediaclear Pd, Histex, Histex Pd Drops New Formulation
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 10849
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
No matching Drugs@FDA applications.
Official labeling on DailyMed
- TRIPROLIDINE HYDROCHLORIDE SYRUP [WESTMINSTER PHARMACEUTICALS, LLC] · version 8 · 2026-08-17
- TRIPROLIDINE HYDROCHLORIDE SYRUP [WESTMINSTER PHARMACEUTICALS, LLC] · version 1 · 2026-08-14
- CHILDRENS PEDIACLEAR PD (TRIPROLIDINE HYDROCHLORIDE) LIQUID [GM PHARMACEUTICALS, INC] · version 9 · 2025-10-06
- HISTEX PD DROPS NEW FORMULATION (TRIPROLIDINE HYDROCHLORIDE) SYRUP [ALLEGIS PHARMACEUTICALS, LLC] · version 3 · 2025-01-10
- HISTEX (TRIPROLIDINE HYDROCHLORIDE) SYRUP [ALLEGIS PHARMACEUTICALS, LLC] · version 4 · 2024-01-10
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.