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FDA ANDA · ANDA072220

CLORAZEPATE DIPOTASSIUM

Sponsor: AUROLIFE PHARMA LLC

APPLICATION
ANDA072220
TYPE
ANDA
ORIGINAL APPROVAL
1988-08-26
LATEST ACTION
2016-12-16
ROUTE
ORAL
DOSAGE FORM
CAPSULE
MARKETING STATUS
Discontinued

Products

CLORAZEPATE DIPOTASSIUMDiscontinued
CLORAZEPATE DIPOTASSIUM 7.5MG · CAPSULE · ORAL

Approval history

2016-12-16Labeling · Supplement 10 · standardAP
1999-08-24Labeling · Supplement 4AP
1990-09-05Labeling · Supplement 1AP
1988-08-26OriginalAP
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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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