Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 083304
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
04/23/1973 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
11/22/2004 SUPPL-43 Labeling

Label is not available on this site.

04/25/2001 SUPPL-41 Manufacturing (CMC)-Control

Label is not available on this site.

01/28/1991 SUPPL-39 Manufacturing (CMC)

Label is not available on this site.

06/29/1990 SUPPL-37 Manufacturing (CMC)

Label is not available on this site.

02/08/1989 SUPPL-36 Labeling

Label is not available on this site.

10/25/1988 SUPPL-35 Labeling

Label is not available on this site.

09/23/1988 SUPPL-34 Manufacturing (CMC)

Label is not available on this site.

09/23/1988 SUPPL-33 Manufacturing (CMC)

Label is not available on this site.

12/12/1985 SUPPL-31 Manufacturing (CMC)

Label is not available on this site.

05/14/1985 SUPPL-30 Manufacturing (CMC)

Label is not available on this site.

05/14/1985 SUPPL-29 Manufacturing (CMC)

Label is not available on this site.

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