NDC 49884-335-01
fluoxetine hydrochloride 10 mg/1
fluoxetine hydrochloride · TABLET, COATED
fluoxetine hydrochloride is a tablet, coated containing fluoxetine hydrochloride at a strength of 10 mg/1. Manufactured by Endo USA, Inc..
Key Facts
- Brand Name
- fluoxetine hydrochloride
- Generic Name
- fluoxetine hydrochloride
- NDC Code (Package)
49884-335-01- NDC Code (Product)
49884-335- Manufacturer
- Endo USA, Inc.
- Strength
- 10 mg/1
- Dosage Form
- TABLET, COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA203836
- Marketing Start
- 08/22/2016
Recall History
No Recall HistoryView Full Drug Page
fluoxetine hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.