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FDA ANDA · ANDA085252

MECLIZINE HYDROCHLORIDE

Sponsor: ABC HOLDING

APPLICATION
ANDA085252
TYPE
ANDA
ORIGINAL APPROVAL
1977-02-15
LATEST ACTION
1990-11-30
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

MECLIZINE HYDROCHLORIDEDiscontinued
MECLIZINE HYDROCHLORIDE 25MG · TABLET · ORAL

Approval history

1990-11-30Labeling · Supplement 41AP
1988-06-27Manufacturing (CMC) · Supplement 40AP
1984-04-09Manufacturing (CMC) · Supplement 38AP
1983-06-29Manufacturing (CMC) · Supplement 37AP
1977-02-15OriginalAP
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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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