NDC 80725-712-04
AVODART .5 mg/1
dutasteride · CAPSULE, LIQUID FILLED
AVODART is a capsule, liquid filled containing dutasteride at a strength of .5 mg/1. Manufactured by Waylis Therapeutics LLC.
Key Facts
- Brand Name
- AVODART
- Generic Name
- dutasteride
- NDC Code (Package)
80725-712-04- 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 HistoryView Full Drug Page
AVODART — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.