APPLICATION
NDA009008
TYPE
NDA
ORIGINAL APPROVAL
1953-04-30
LATEST ACTION
1979-09-24
ROUTE
INTRAUTERINE
DOSAGE FORM
SOLUTION
MARKETING STATUS
Discontinued
Products
SALPIXDiscontinued
ACETRIZOATE SODIUM 53% · SOLUTION · INTRAUTERINE
Approval history
1979-09-24Labeling · Supplement 12AP
1979-09-13Labeling · Supplement 11AP
1979-01-05Labeling · Supplement 4AP
1978-04-26Labeling · Supplement 7AP
1953-04-30Type 4 - New Combination · Original · standardAP
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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