NDC 55111-284-48
Fluoxetine hydrochloride 90 mg/1
Fluoxetine Hydrochloride · CAPSULE, DELAYED RELEASE PELLETS
Fluoxetine hydrochloride is a capsule, delayed release pellets containing fluoxetine hydrochloride at a strength of 90 mg/1. Manufactured by Dr.Reddy's Laboratories Limited.
Key Facts
- Brand Name
- Fluoxetine hydrochloride
- Generic Name
- Fluoxetine Hydrochloride
- NDC Code (Package)
55111-284-48- NDC Code (Product)
55111-284- Manufacturer
- Dr.Reddy's Laboratories Limited
- Strength
- 90 mg/1
- Dosage Form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Marketing Status
- Application #
- ANDA078572
- Marketing Start
- 03/24/2010
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.