APPLICATION
ANDA070566
TYPE
ANDA
ORIGINAL APPROVAL
1986-06-09
LATEST ACTION
2001-04-09
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
NITROPRESSDiscontinued
SODIUM NITROPRUSSIDE 50MG/VIAL · INJECTABLE · INJECTION
Approval history
2001-04-09Manufacturing (CMC) · Supplement 17AP
2000-04-04Manufacturing (CMC) · Supplement 16AP
1995-05-10Manufacturing (CMC) · Supplement 12AP
1995-02-10Manufacturing (CMC) · Supplement 11AP
1994-12-30Labeling · Supplement 13AP
1994-02-24Manufacturing (CMC) · Supplement 10AP
1992-10-30Manufacturing (CMC) · Supplement 9AP
1992-04-09Labeling · Supplement 8AP
1990-12-27Labeling · Supplement 7AP
1990-03-14Labeling · Supplement 6AP
1989-01-31Manufacturing (CMC) · Supplement 5AP
1988-09-19Manufacturing (CMC) · Supplement 2AP
1988-09-19Manufacturing (CMC) · Supplement 3AP
1988-09-19Manufacturing (CMC) · Supplement 4AP
1986-08-13Manufacturing (CMC) · Supplement 1AP
1986-06-09OriginalAP
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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