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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 071639
Company: VINTAGE PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
IBUPROFEN IBUPROFEN 200MG 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
02/02/1988 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
07/25/1991 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

05/03/1991 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

06/09/1988 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

06/09/1988 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

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