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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 089497
Company: PAR PHARM
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
IMIPRAMINE HYDROCHLORIDE IMIPRAMINE HYDROCHLORIDE 25MG TABLET;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
07/14/1987 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
10/02/1997 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

03/25/1996 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

03/25/1996 SUPPL-10 Manufacturing (CMC)

Label is not available on this site.

03/25/1996 SUPPL-9 Labeling

Label is not available on this site.

10/23/1995 SUPPL-8 Labeling

Label is not available on this site.

11/05/1993 SUPPL-7 Labeling

Label is not available on this site.

01/07/1991 SUPPL-6 Labeling

Label is not available on this site.

08/19/1988 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

08/19/1988 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

08/19/1988 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

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