Psorizide Ultra 1 [hp_X]/1
Potassium Bromide, Nickel Sulfate, and Zinc Bromide · TABLET · PLYMOUTH HEALTHCARE PRODUCTS LLC
Psorizide Ultra is a tablet containing potassium bromide, nickel sulfate, and zinc bromide at 1 [hp_X]/1, taken oral. Manufactured by PLYMOUTH HEALTHCARE PRODUCTS LLC.
Key Facts
- Brand Name
- Psorizide Ultra
- Generic Name
- Potassium Bromide, Nickel Sulfate, and Zinc Bromide
- NDC Code (Product)
61480-124- Manufacturer
- PLYMOUTH HEALTHCARE PRODUCTS LLC
- Strength
- 1 [hp_X]/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Marketing Start
- 10/01/1997
Recall History
No Recall HistoryFrequently Asked Questions
What is Psorizide Ultra used for?
Psorizide Ultra contains Potassium Bromide, Nickel Sulfate, and Zinc Bromide. It is a tablet taken oral. Consult your doctor for specific uses.
Is Psorizide Ultra a controlled substance?
Psorizide Ultra is not classified as a controlled substance by the DEA.
What is the generic name for Psorizide Ultra?
The generic name for Psorizide Ultra is Potassium Bromide, Nickel Sulfate, and Zinc Bromide. There are no other listed brand versions of Potassium Bromide, Nickel Sulfate, and Zinc Bromide.
What is the NDC code for Psorizide Ultra 1 [hp_X]/1?
The NDC (National Drug Code) for Psorizide Ultra 1 [hp_X]/1 is 61480-124, listed by PLYMOUTH HEALTHCARE PRODUCTS LLC.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)