Duratuss AC 10 mg/5mL
Codeine Phosphate, Dexbrompheniramine Maleate · LIQUID · Poly Pharmaceuticals, Inc.
Duratuss AC is a liquid containing codeine phosphate, dexbrompheniramine maleate at 10 mg/5mL, taken oral. Manufactured by Poly Pharmaceuticals, Inc..
Key Facts
- Brand Name
- Duratuss AC
- Generic Name
- Codeine Phosphate, Dexbrompheniramine Maleate
- NDC Code (Product)
50991-540- Manufacturer
- Poly Pharmaceuticals, Inc.
- Strength
- 10 mg/5mL
- Dosage Form
- LIQUID
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule V (Controlled)
- Application #
- M012
- Marketing Start
- 09/08/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is Duratuss AC used for?
Duratuss AC contains Codeine Phosphate, Dexbrompheniramine Maleate. It is a liquid taken oral. Consult your doctor for specific uses.
Is Duratuss AC a controlled substance?
Yes, Duratuss AC is classified as CV under the DEA Controlled Substances Act.
What is the generic name for Duratuss AC?
The generic name for Duratuss AC is Codeine Phosphate, Dexbrompheniramine Maleate. There are no other listed brand versions of Codeine Phosphate, Dexbrompheniramine Maleate.
What is the NDC code for Duratuss AC 10 mg/5mL?
The NDC (National Drug Code) for Duratuss AC 10 mg/5mL is 50991-540, 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)