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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 076099
Company: HIKMA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CARBOPLATIN CARBOPLATIN 50MG/VIAL INJECTABLE;INJECTION Discontinued None No No
CARBOPLATIN CARBOPLATIN 150MG/VIAL INJECTABLE;INJECTION Discontinued None No No
CARBOPLATIN CARBOPLATIN 450MG/VIAL INJECTABLE;INJECTION 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
10/14/2004 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
03/02/2012 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

09/07/2011 SUPPL-4 Labeling-Package Insert

Label is not available on this site.

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