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Drug profile · INN

duloxetine hydrochloride

DULOXETINE HYDROCHLORIDE

approved
US status
approved
Patents linked
2
News articles
0

Quick answer

duloxetine hydrochloride (DULOXETINE HYDROCHLORIDE) is an FDA-listed pharmaceutical active ingredient. Associated with Sunshine Biopharma. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN duloxetine hydrochloride
Brand DULOXETINE HYDROCHLORIDE
Route ORAL
Formulation CAPSULE, DELAYED RELEASE
Originator Sunshine Biopharma

Related patents

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  1. US 7759500

    2-(N-methyl-propanamine)-3-(2-naphthol)thiophene, an impurity of duloxetine hydrochloride

    Expires Mon Jul 15 2030 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

  2. US 7534900

    Process for the purification of duloxetine hydrochloride

    Expires Mon May 14 2029 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is duloxetine hydrochloride?

duloxetine hydrochloride (DULOXETINE HYDROCHLORIDE) is an FDA-listed pharmaceutical active ingredient. Associated with Sunshine Biopharma. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for duloxetine hydrochloride?

DULOXETINE HYDROCHLORIDE is a marketed brand name for duloxetine hydrochloride. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of duloxetine hydrochloride?

duloxetine hydrochloride has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.