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FDA NDA · NDA017569

RENOQUID

Sponsor: GLENWOOD

APPLICATION
NDA017569
TYPE
NDA
ORIGINAL APPROVAL
1975-09-12
LATEST ACTION
1986-12-16
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

RENOQUIDDiscontinued
SULFACYTINE 250MG · TABLET · ORAL

Approval history

1986-12-16Labeling · Supplement 6 · priorityAP
1981-04-09Manufacturing (CMC) · Supplement 5 · priorityAP
1979-10-23Manufacturing (CMC) · Supplement 4 · priorityAP
1978-07-05Manufacturing (CMC) · Supplement 3 · priorityAP
1978-01-12Manufacturing (CMC) · Supplement 2 · priorityAP
1976-11-22Manufacturing (CMC) · Supplement 1 · priorityAP
1975-09-12Type 1 - New Molecular Entity · Original · priorityAP
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