Fusarium moniliforme .05 g/mL
Fusarium moniliforme · SOLUTION · Greer Laboratories, Inc.
Fusarium moniliforme is a solution containing fusarium moniliforme at .05 g/mL, taken intradermal. Manufactured by Greer Laboratories, Inc..
Key Facts
- Brand Name
- Fusarium moniliforme
- Generic Name
- Fusarium moniliforme
- NDC Code (Product)
22840-5618- Manufacturer
- Greer Laboratories, Inc.
- Strength
- .05 g/mL
- Dosage Form
- SOLUTION
- Route
- INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
- Marketing Status
- Application #
- BLA101833
- Marketing Start
- 09/15/1981
Recall History
No Recall HistoryFrequently Asked Questions
What is Fusarium moniliforme used for?
Fusarium moniliforme contains Fusarium moniliforme. It is a solution taken intradermal. Consult your doctor for specific uses.
Is Fusarium moniliforme a controlled substance?
Fusarium moniliforme is not classified as a controlled substance by the DEA.
What is the generic name for Fusarium moniliforme?
The generic name for Fusarium moniliforme is Fusarium moniliforme. There are no other listed brand versions of Fusarium moniliforme.
What is the NDC code for Fusarium moniliforme .05 g/mL?
The NDC (National Drug Code) for Fusarium moniliforme .05 g/mL is 22840-5618, listed by Greer Laboratories, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)