Drugplain

Duloxetine Hydrochloride 60 mg/1

Duloxetine Hydrochloride · CAPSULE, DELAYED RELEASE · Macleods Pharmaceuticals Limited

No Recall History
Plain English

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 (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 History

Frequently Asked Questions

What is Duloxetine Hydrochloride used for?

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.

Is Duloxetine Hydrochloride a controlled substance?

Duloxetine Hydrochloride is not classified as a controlled substance by the DEA.

What is the generic name for Duloxetine Hydrochloride?

The generic name for Duloxetine Hydrochloride is Duloxetine Hydrochloride. There are 12 other brand versions of Duloxetine Hydrochloride.

What is the NDC code for Duloxetine Hydrochloride 60 mg/1?

The NDC (National Drug Code) for Duloxetine Hydrochloride 60 mg/1 is 33342-162, listed by Macleods Pharmaceuticals Limited.