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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 202045
Company: APOTEX
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE EQ 20MG BASE CAPSULE, DELAYED REL PELLETS;ORAL Discontinued None No No
DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE EQ 30MG BASE CAPSULE, DELAYED REL PELLETS;ORAL Discontinued None No No
DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE EQ 60MG BASE CAPSULE, DELAYED REL PELLETS;ORAL Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
06/11/2014 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
01/31/2024 SUPPL-17 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

05/02/2023 SUPPL-16 Labeling-Container/Carton Labels, Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

05/02/2023 SUPPL-14 Labeling-Package Insert

Label is not available on this site.

05/02/2023 SUPPL-13 Labeling-Package Insert

Label is not available on this site.

05/02/2023 SUPPL-11 Labeling-Container/Carton Labels, Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

07/10/2017 SUPPL-10 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

07/10/2017 SUPPL-9 Labeling-Package Insert

Label is not available on this site.

07/10/2017 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

07/10/2017 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

07/10/2017 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

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