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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 087537
Company: PAR PHARM
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ISOSORBIDE DINITRATE ISOSORBIDE DINITRATE 20MG 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
10/02/1987 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
05/24/2002 SUPPL-20 Labeling

Label is not available on this site.

12/07/1999 SUPPL-19 Labeling

Label is not available on this site.

06/23/1997 SUPPL-18 Labeling

Label is not available on this site.

07/11/1996 SUPPL-17 Labeling

Label is not available on this site.

11/01/1991 SUPPL-16 Labeling

Label is not available on this site.

03/16/1994 SUPPL-15 Manufacturing (CMC)

Label is not available on this site.

03/16/1994 SUPPL-14 Manufacturing (CMC)

Label is not available on this site.

12/04/1984 SUPPL-8 Manufacturing (CMC)

Label is not available on this site.

09/28/1982 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

ISOSORBIDE DINITRATE

TABLET;ORAL; 20MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
ISOSORBIDE DINITRATE ISOSORBIDE DINITRATE 20MG TABLET;ORAL Prescription No AB 088088 HIKMA INTL PHARMS
ISOSORBIDE DINITRATE ISOSORBIDE DINITRATE 20MG TABLET;ORAL Prescription No AB 087537 PAR PHARM
ISOSORBIDE DINITRATE ISOSORBIDE DINITRATE 20MG TABLET;ORAL Prescription No AB 215723 RUBICON
ISOSORBIDE DINITRATE ISOSORBIDE DINITRATE 20MG TABLET;ORAL Prescription No AB 089367 SANDOZ
ISOSORBIDE DINITRATE ISOSORBIDE DINITRATE 20MG TABLET;ORAL Prescription No AB 213057 ZYDUS
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