AVODART .5 mg/1
dutasteride · CAPSULE, LIQUID FILLED · Waylis Therapeutics LLC
No Recall History
Plain English
AVODART is a capsule, liquid filled containing dutasteride at .5 mg/1, taken oral. Manufactured by Waylis Therapeutics LLC.
Key Facts
- Brand Name
- AVODART
- Generic Name
- dutasteride
- NDC Code (Product)
80725-712- Manufacturer
- Waylis Therapeutics LLC
- Strength
- .5 mg/1
- Dosage Form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Marketing Status
- Application #
- NDA021319
- Drug Class
- 5-alpha Reductase Inhibitor [EPC]
- Marketing Start
- 12/15/2022
Recall History
No Recall HistoryFrequently Asked Questions
What is AVODART used for?
AVODART contains dutasteride. It is a capsule, liquid filled taken oral. Consult your doctor for specific uses.
Is AVODART a controlled substance?
AVODART is not classified as a controlled substance by the DEA.
What is the generic name for AVODART?
The generic name for AVODART is dutasteride. There are 12 other brand versions of dutasteride.
What is the NDC code for AVODART .5 mg/1?
The NDC (National Drug Code) for AVODART .5 mg/1 is 80725-712, listed by Waylis Therapeutics LLC.