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FDA ANDA · ANDA084181

MEPROBAMATE

Sponsor: IVAX SUB TEVA PHARMS

APPLICATION
ANDA084181
TYPE
ANDA
ORIGINAL APPROVAL
1974-04-29
LATEST ACTION
1974-04-29
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

MEPROBAMATEDiscontinued
MEPROBAMATE 600MG · TABLET · ORAL

Approval history

1974-04-29OriginalAP
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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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