Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 070965
Company: WATSON LABS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CLONIDINE HYDROCHLORIDE CLONIDINE HYDROCHLORIDE 0.1MG 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
07/01/1986 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
09/07/1999 SUPPL-18 Manufacturing (CMC)

Label is not available on this site.

01/31/1997 SUPPL-16 Labeling

Label is not available on this site.

05/15/1991 SUPPL-15 Labeling

Label is not available on this site.

01/28/1991 SUPPL-14 Manufacturing (CMC)

Label is not available on this site.

05/31/1991 SUPPL-13 Manufacturing (CMC)

Label is not available on this site.

06/29/1990 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

04/07/1988 SUPPL-11 Labeling

Label is not available on this site.

03/25/1988 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

12/09/1987 SUPPL-8 Manufacturing (CMC)

Label is not available on this site.

05/15/1987 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

11/12/1986 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

11/12/1986 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

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