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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 077730
Company: PLIVA HRVATSKA DOO
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PRAVASTATIN SODIUM PRAVASTATIN SODIUM 10MG TABLET;ORAL Discontinued None No No
PRAVASTATIN SODIUM PRAVASTATIN SODIUM 20MG TABLET;ORAL Discontinued None No No
PRAVASTATIN SODIUM PRAVASTATIN SODIUM 30MG TABLET;ORAL Discontinued None No No
PRAVASTATIN SODIUM PRAVASTATIN SODIUM 80MG TABLET; ORAL None (Tentative Approval) None No No
PRAVASTATIN SODIUM PRAVASTATIN SODIUM 40MG 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
11/21/2006 ORIG-1 Tentative Approval

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