NDC 33342-162-07
Duloxetine Hydrochloride 60 mg/1
Duloxetine Hydrochloride · CAPSULE, DELAYED RELEASE
Duloxetine hydrochloride is a prescription medication taken by mouth that belongs to a class of antidepressants called serotonin-norepinephrine reuptake inhibitors (SNRIs), commonly used to treat depression, anxiety, chronic pain conditions, and fibromyalgia. The delayed-release capsule formulation allows the medication to be absorbed in the small intestine rather than the stomach.
Key Facts
- Brand Name
- Duloxetine Hydrochloride
- Generic Name
- Duloxetine Hydrochloride
- NDC Code (Package)
33342-162-07- NDC Code (Product)
33342-162- Manufacturer
- Macleods Pharmaceuticals Limited
- Strength
- 60 mg/1
- Dosage Form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA204815
- Marketing Start
- 03/24/2017
Recall History
No Recall HistoryView Full Drug Page
Duloxetine Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.