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FDA ANDA · ANDA088409

HYDROXYZINE HYDROCHLORIDE

Sponsor: MUTUAL PHARM

APPLICATION
ANDA088409
TYPE
ANDA
ORIGINAL APPROVAL
1983-11-15
LATEST ACTION
1998-12-01
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

HYDROXYZINE HYDROCHLORIDEDiscontinued
HYDROXYZINE HYDROCHLORIDE 10MG · TABLET · ORAL

Approval history

1998-12-01Manufacturing (CMC) · Supplement 14AP
1994-12-23Manufacturing (CMC) · Supplement 13AP
1994-10-11Manufacturing (CMC) · Supplement 12AP
1992-04-03Manufacturing (CMC) · Supplement 9AP
1992-04-03Manufacturing (CMC) · Supplement 11AP
1987-12-10Manufacturing (CMC) · Supplement 6AP
1987-03-25Manufacturing (CMC) · Supplement 5AP
1985-03-26Manufacturing (CMC) · Supplement 3AP
1984-11-20Manufacturing (CMC) · Supplement 2AP
1983-11-15OriginalAP
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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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