APPLICATION
ANDA070886
TYPE
ANDA
ORIGINAL APPROVAL
1988-08-31
LATEST ACTION
1998-03-25
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription
Products
CLONIDINE HYDROCHLORIDEPrescription
CLONIDINE HYDROCHLORIDE 0.1MG · TABLET · ORAL
CLONIDINE HYDROCHLORIDEPrescription
CLONIDINE HYDROCHLORIDE 0.3MG · TABLET · ORAL
CLONIDINE HYDROCHLORIDEPrescription
CLONIDINE HYDROCHLORIDE 0.2MG · TABLET · ORAL
Approval history
1998-03-25Labeling · Supplement 5AP
1998-03-02Manufacturing (CMC) · Supplement 6AP
1995-02-01Manufacturing (CMC) · Supplement 4AP
1992-03-04Manufacturing (CMC) · Supplement 3AP
1988-08-31OriginalAP
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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