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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 084936
Company: SANDOZ
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
IMIPRAMINE HYDROCHLORIDE IMIPRAMINE HYDROCHLORIDE 10MG TABLET;ORAL Prescription AB 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
04/20/1976 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
05/24/2023 SUPPL-109 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

02/02/2016 SUPPL-108 Labeling-Package Insert

Label is not available on this site.

07/17/2014 SUPPL-107 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

03/10/2008 SUPPL-102 Labeling

Label is not available on this site.

06/25/2007 SUPPL-101 Labeling

Label is not available on this site.

06/15/2005 SUPPL-100 Labeling

Label is not available on this site.

04/19/2002 SUPPL-97 Manufacturing (CMC)-Control

Label is not available on this site.

05/09/2001 SUPPL-96 Manufacturing (CMC)-Control

Label is not available on this site.

10/16/2001 SUPPL-95 Manufacturing (CMC)-Control

Label is not available on this site.

10/31/2000 SUPPL-94 Manufacturing (CMC)-Control

Label is not available on this site.

05/11/1999 SUPPL-93 Labeling

Label is not available on this site.

05/05/1999 SUPPL-92 Manufacturing (CMC)

Label is not available on this site.

02/09/2007 SUPPL-91 Labeling

Label is not available on this site.

03/21/1995 SUPPL-86 Labeling

Label is not available on this site.

04/06/1995 SUPPL-85 Manufacturing (CMC)

Label is not available on this site.

03/11/1994 SUPPL-84 Labeling

Label is not available on this site.

11/07/1989 SUPPL-83 Labeling

Label is not available on this site.

02/22/1988 SUPPL-82 Manufacturing (CMC)

Label is not available on this site.

01/19/1988 SUPPL-81 Manufacturing (CMC)

Label is not available on this site.

01/19/1988 SUPPL-80 Manufacturing (CMC)

Label is not available on this site.

01/19/1988 SUPPL-79 Manufacturing (CMC)

Label is not available on this site.

01/19/1988 SUPPL-78 Manufacturing (CMC)

Label is not available on this site.

01/19/1988 SUPPL-77 Manufacturing (CMC)

Label is not available on this site.

01/16/1986 SUPPL-73 Manufacturing (CMC)

Label is not available on this site.

12/27/1985 SUPPL-72 Manufacturing (CMC)

Label is not available on this site.

10/21/1983 SUPPL-66 Manufacturing (CMC)

Label is not available on this site.

07/19/1983 SUPPL-64 Manufacturing (CMC)

Label is not available on this site.

12/10/1982 SUPPL-62 Manufacturing (CMC)

Label is not available on this site.

06/09/1982 SUPPL-58 Manufacturing (CMC)

Label is not available on this site.

IMIPRAMINE HYDROCHLORIDE

TABLET;ORAL; 10MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
IMIPRAMINE HYDROCHLORIDE IMIPRAMINE HYDROCHLORIDE 10MG TABLET;ORAL Prescription No AB 040903 LEADING
IMIPRAMINE HYDROCHLORIDE IMIPRAMINE HYDROCHLORIDE 10MG TABLET;ORAL Prescription No AB 040751 OXFORD PHARMS
IMIPRAMINE HYDROCHLORIDE IMIPRAMINE HYDROCHLORIDE 10MG TABLET;ORAL Prescription No AB 084936 SANDOZ
IMIPRAMINE HYDROCHLORIDE IMIPRAMINE HYDROCHLORIDE 10MG TABLET;ORAL Prescription No AB 088292 STRIDES PHARMA
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