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 HistoryFrequently 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)