Drugplain

TRIPROLIDINE HYDROCHLORIDE .938 mg/mL

TRIPROLIDINE HYDROCHLORIDE · SYRUP · Westminster Pharmaceuticals, LLC

No Recall History
Plain English

TRIPROLIDINE HYDROCHLORIDE is a syrup containing triprolidine hydrochloride at .938 mg/mL, taken oral. Manufactured by Westminster Pharmaceuticals, LLC.

Key Facts

Brand Name
TRIPROLIDINE HYDROCHLORIDE
Generic Name
TRIPROLIDINE HYDROCHLORIDE
NDC Code (Product)
69367-253
Manufacturer
Westminster Pharmaceuticals, LLC
Strength
.938 mg/mL
Dosage Form
SYRUP
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
03/09/2020

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

psoriatic arthropathy122 reports
oedema121 reports
pericarditis121 reports
pemphigus120 reports
type 2 diabetes mellitus120 reports
joint swelling119 reports
pyrexia119 reports
sinusitis117 reports
urticaria116 reports
injury115 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes

Dosage & Administration

Directions do not exceed recommended dosage. use only the enclosed dropper do not use enclosed dropper for any other drug product. AGE DOSE Adults & Children 12 years of age or older: 2.67 mL (2.5 milligrams) every 4 to 6 hours, not to exceed 10.67 mL (10 milligrams) in 24 hours, or as directed by a doctor. Children 6 to under 12 years of age: 1.33 mL (1.25 milligrams) every 4 to 6 hours, not to exceed 5.33 mL (5 milligrams) in 24 hours, or as directed by a doctor. Children under 6 years of age: consult a doctor.

Warnings

Warnings Do not exceed recommended dosage. Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis trouble urinating due to an enlarged prostate gland Ask a doctor before use if you are taking sedatives or tranquilizers When using this product excitability may occur, especially in children may cause drowsiness alcohol, sedatives and tranquilizers may increase the drowsiness effect avoid alcoholic beverages use caution when driving a motor vehicle or operating machinery Stop use and ask a doctor if new symptoms occur If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Frequently Asked Questions

What is TRIPROLIDINE HYDROCHLORIDE used for?

TRIPROLIDINE HYDROCHLORIDE contains TRIPROLIDINE HYDROCHLORIDE. It is a syrup taken oral. Consult your doctor for specific uses.

Is TRIPROLIDINE HYDROCHLORIDE a controlled substance?

TRIPROLIDINE HYDROCHLORIDE is not classified as a controlled substance by the DEA.

What is the generic name for TRIPROLIDINE HYDROCHLORIDE?

The generic name for TRIPROLIDINE HYDROCHLORIDE is TRIPROLIDINE HYDROCHLORIDE. There are 3 other brand versions of TRIPROLIDINE HYDROCHLORIDE.

What is the NDC code for TRIPROLIDINE HYDROCHLORIDE .938 mg/mL?

The NDC (National Drug Code) for TRIPROLIDINE HYDROCHLORIDE .938 mg/mL is 69367-253, listed by Westminster Pharmaceuticals, LLC.

Product NDC

69367-253

Package NDC

69367-253-30

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)