APPLICATION
NDA011679
TYPE
NDA
ORIGINAL APPROVAL
1959-09-23
LATEST ACTION
2001-09-17
ROUTE
RECTAL
DOSAGE FORM
SUSPENSION
MARKETING STATUS
Discontinued
Products
PENTOTHALDiscontinued
THIOPENTAL SODIUM 400MG/GM · SUSPENSION · RECTAL
Approval history
2001-09-17Labeling · Supplement 17AP
1995-03-30Labeling · Supplement 18 · standardAP
1984-02-15Labeling · Supplement 13AP
1977-01-24Labeling · Supplement 10AP
1976-09-10Labeling · Supplement 9AP
1975-10-20Labeling · Supplement 7AP
1971-08-30Labeling · Supplement 6AP
1959-09-23Type 1 - New Molecular Entity · Original · priorityAP
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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