APPLICATION
ANDA070317
TYPE
ANDA
ORIGINAL APPROVAL
1987-06-09
LATEST ACTION
2013-01-16
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
CLONIDINE HYDROCHLORIDEDiscontinued
CLONIDINE HYDROCHLORIDE 0.2MG · TABLET · ORAL
CLONIDINE HYDROCHLORIDEDiscontinued
CLONIDINE HYDROCHLORIDE 0.3MG · TABLET · ORAL
CLONIDINE HYDROCHLORIDEDiscontinued
CLONIDINE HYDROCHLORIDE 0.1MG · TABLET · ORAL
Approval history
2013-01-16Labeling · Supplement 23 · standardAP
1998-02-05Manufacturing (CMC) · Supplement 9AP
1997-07-15Labeling · Supplement 8AP
1995-02-24Manufacturing (CMC) · Supplement 7AP
1993-10-01Manufacturing (CMC) · Supplement 5AP
1991-07-29Manufacturing (CMC) · Supplement 1AP
1991-03-22Labeling · Supplement 4AP
1990-01-31Manufacturing (CMC) · Supplement 3AP
1987-06-09OriginalAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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