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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 075668
Company: ANI PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
NIZATIDINE NIZATIDINE 150MG CAPSULE;ORAL Discontinued None No No
NIZATIDINE NIZATIDINE 300MG CAPSULE;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
09/12/2002 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
06/24/2009 SUPPL-6 Labeling

Label is not available on this site.

05/21/2009 SUPPL-2 Labeling

Label is not available on this site.

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