Cuadriderma 500 [iU]/g
Bacitracin Zinc, Polymyxin B Sulfate, Neomycin Sulfate, and PRAMOXINE HYDROCHLORIDE · OINTMENT · ProMex LLC
Cuadriderma is a ointment containing bacitracin zinc, polymyxin b sulfate, neomycin sulfate, and pramoxine hydrochloride at 500 [iU]/g, taken topical. Manufactured by ProMex LLC.
Key Facts
- Brand Name
- Cuadriderma
- Generic Name
- Bacitracin Zinc, Polymyxin B Sulfate, Neomycin Sulfate, and PRAMOXINE HYDROCHLORIDE
- NDC Code (Product)
58988-1170- Manufacturer
- ProMex LLC
- Strength
- 500 [iU]/g
- Dosage Form
- OINTMENT
- Route
- TOPICAL
- Marketing Status
- Application #
- M004
- Marketing Start
- 05/31/2013
Recall History
No Recall HistoryFrequently Asked Questions
What is Cuadriderma used for?
Cuadriderma contains Bacitracin Zinc, Polymyxin B Sulfate, Neomycin Sulfate, and PRAMOXINE HYDROCHLORIDE. It is a ointment taken topical. Consult your doctor for specific uses.
Is Cuadriderma a controlled substance?
Cuadriderma is not classified as a controlled substance by the DEA.
What is the generic name for Cuadriderma?
The generic name for Cuadriderma is Bacitracin Zinc, Polymyxin B Sulfate, Neomycin Sulfate, and PRAMOXINE HYDROCHLORIDE. There are no other listed brand versions of Bacitracin Zinc, Polymyxin B Sulfate, Neomycin Sulfate, and PRAMOXINE HYDROCHLORIDE.
What is the NDC code for Cuadriderma 500 [iU]/g?
The NDC (National Drug Code) for Cuadriderma 500 [iU]/g is 58988-1170, listed by ProMex LLC.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)