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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 071215
Company: MCNEIL
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
MEDIPREN 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
06/26/1986 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
02/14/1989 SUPPL-19 Manufacturing (CMC)

Label is not available on this site.

09/09/1988 SUPPL-17 Labeling

Label is not available on this site.

04/07/1988 SUPPL-16 Manufacturing (CMC)

Label is not available on this site.

04/07/1988 SUPPL-15 Manufacturing (CMC)

Label is not available on this site.

04/07/1988 SUPPL-14 Manufacturing (CMC)

Label is not available on this site.

10/20/1987 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

09/10/1987 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

09/10/1987 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

11/05/1986 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

11/05/1986 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

11/05/1986 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

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