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FDA ANDA · ANDA087776

IMIPRAMINE HYDROCHLORIDE

Sponsor: USL PHARMA

APPLICATION
ANDA087776
TYPE
ANDA
ORIGINAL APPROVAL
1982-02-10
LATEST ACTION
1987-02-19
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

IMIPRAMINE HYDROCHLORIDEDiscontinued
IMIPRAMINE HYDROCHLORIDE 25MG · TABLET · ORAL

Approval history

1987-02-19Manufacturing (CMC) · Supplement 5AP
1985-05-10Manufacturing (CMC) · Supplement 2AP
1982-02-10OriginalAP
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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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