Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 079010
Company: VINTAGE
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATE EQ 15MG BASE/5ML SOLUTION;ORAL Prescription AA 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
05/26/2009 ORIG-1 Approval

Label is not available on this site.

PREDNISOLONE SODIUM PHOSPHATE

SOLUTION;ORAL; EQ 15MG BASE/5ML
TE Code = AA

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATE EQ 15MG BASE/5ML SOLUTION;ORAL Prescription No AA 076913 PHARM ASSOC
PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATE EQ 15MG BASE/5ML SOLUTION;ORAL Prescription No AA 079010 VINTAGE
PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATE EQ 15MG BASE/5ML SOLUTION;ORAL Prescription No AA 076895 WOCKHARDT BIO AG

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