DURATUSS DM 1 mg/5mL
Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide and Pseudoephedrine Hydrochloride · LIQUID · Poly Pharmaceuticals, Inc.
DURATUSS DM is a liquid containing dexbrompheniramine maleate, dextromethorphan hydrobromide and pseudoephedrine hydrochloride at 1 mg/5mL, taken oral. Manufactured by Poly Pharmaceuticals, Inc..
Key Facts
- Brand Name
- DURATUSS DM
- Generic Name
- Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide and Pseudoephedrine Hydrochloride
- NDC Code (Product)
50991-142- Manufacturer
- Poly Pharmaceuticals, Inc.
- Strength
- 1 mg/5mL
- Dosage Form
- LIQUID
- Route
- ORAL
- Marketing Status
- Application #
- M012
- Marketing Start
- 10/15/2025
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies: runny nose sneezing itching of nose or throat itchy, watery eyes cough due to minor throat and bronchial irritation nasal congestion reduces swelling of nasal passages
Dosage & Administration
Directions Do not exceed recommended dosage. Adults and children 12 years of age and over: 2 teaspoonful (10 mL) every 4 to 6 hours, not to exceed 8 teaspoonfuls in a 24 hours Children 6 to under 12 years of age: 1 teaspoonful (5 mL) every 4 to 6 hours, not to exceed 4 teaspoonfuls in 24 hours Children under 6 years of age: Consult a doctor.
Warnings
Warnings Do not exceed recommended dosage. Do not use this product if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have a breathing problem such as emphysema or chronic bronchitis glaucoma trouble urinating due to an enlarged prostate gland a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema a cough that occurs with too much phlegm (mucus) heart disease high blood pressure thyroid disease diabetes Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers. When using this product excitability may occur, especially in children may cause marked drowsiness avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase the drowsiness effect be careful when driving a motor vehicle or operating machinery Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur cough or nasal congestion persists for …
Frequently Asked Questions
What is DURATUSS DM used for?
DURATUSS DM contains Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide and Pseudoephedrine Hydrochloride. It is a liquid taken oral. Consult your doctor for specific uses.
Is DURATUSS DM a controlled substance?
DURATUSS DM is not classified as a controlled substance by the DEA.
What is the generic name for DURATUSS DM?
The generic name for DURATUSS DM is Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide and Pseudoephedrine Hydrochloride. There are no other listed brand versions of Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide and Pseudoephedrine Hydrochloride.
What is the NDC code for DURATUSS DM 1 mg/5mL?
The NDC (National Drug Code) for DURATUSS DM 1 mg/5mL is 50991-142, listed by Poly Pharmaceuticals, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)