Fluoxetine hydrochloride 90 mg/1
Fluoxetine Hydrochloride · CAPSULE, DELAYED RELEASE PELLETS · Dr.Reddy's Laboratories Limited
Fluoxetine hydrochloride is a capsule, delayed release pellets containing fluoxetine hydrochloride at 90 mg/1, taken oral. Manufactured by Dr.Reddy's Laboratories Limited.
Key Facts
- Brand Name
- Fluoxetine hydrochloride
- Generic Name
- Fluoxetine Hydrochloride
- 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 HistoryFrequently Asked Questions
What is Fluoxetine hydrochloride used for?
Fluoxetine hydrochloride contains Fluoxetine Hydrochloride. It is a capsule, delayed release pellets taken oral. Consult your doctor for specific uses.
Is Fluoxetine hydrochloride a controlled substance?
Fluoxetine hydrochloride is not classified as a controlled substance by the DEA.
What is the generic name for Fluoxetine hydrochloride?
The generic name for Fluoxetine hydrochloride is Fluoxetine Hydrochloride. There are 12 other brand versions of Fluoxetine Hydrochloride.
What is the NDC code for Fluoxetine hydrochloride 90 mg/1?
The NDC (National Drug Code) for Fluoxetine hydrochloride 90 mg/1 is 55111-284, listed by Dr.Reddy's Laboratories Limited.