VEOZAH 45 mg/1
fezolinetant · TABLET, FILM COATED · Astellas Pharma US, Inc.
No Recall History
Plain English
VEOZAH is a tablet, film coated containing fezolinetant at 45 mg/1, taken oral. Manufactured by Astellas Pharma US, Inc..
Key Facts
- Brand Name
- VEOZAH
- Generic Name
- fezolinetant
- NDC Code (Product)
0469-2460- Manufacturer
- Astellas Pharma US, Inc.
- Strength
- 45 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA216578
- Drug Class
- Neurokinin 3 Receptor Antagonist [EPC]
- Marketing Start
- 05/16/2023
Recall History
No Recall HistoryFrequently Asked Questions
What is VEOZAH used for?
VEOZAH contains fezolinetant. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is VEOZAH a controlled substance?
VEOZAH is not classified as a controlled substance by the DEA.
What is the generic name for VEOZAH?
The generic name for VEOZAH is fezolinetant. There are no other listed brand versions of fezolinetant.
What is the NDC code for VEOZAH 45 mg/1?
The NDC (National Drug Code) for VEOZAH 45 mg/1 is 0469-2460, listed by Astellas Pharma US, Inc..
Other VEOZAH Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)