Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 085720
Company: WATSON LABS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
MEPROBAMATE MEPROBAMATE 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
07/13/1977 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
08/20/1999 SUPPL-31 Manufacturing (CMC)-Control

Label is not available on this site.

01/21/1999 SUPPL-30 Manufacturing (CMC)

Label is not available on this site.

07/18/1997 SUPPL-29 Manufacturing (CMC)

Label is not available on this site.

07/18/1997 SUPPL-28 Manufacturing (CMC)

Label is not available on this site.

03/26/1997 SUPPL-27 Manufacturing (CMC)

Label is not available on this site.

04/22/1991 SUPPL-26 Labeling

Label is not available on this site.

03/28/1988 SUPPL-22 Labeling

Label is not available on this site.

12/24/1987 SUPPL-20 Manufacturing (CMC)

Label is not available on this site.

07/21/1987 SUPPL-19 Manufacturing (CMC)

Label is not available on this site.

07/21/1987 SUPPL-18 Manufacturing (CMC)

Label is not available on this site.

12/10/1986 SUPPL-16 Manufacturing (CMC)

Label is not available on this site.

12/07/1981 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

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