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FDA NDA · NDA018186

SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINER

Sponsor: B BRAUN

APPLICATION
NDA018186
TYPE
NDA
ORIGINAL APPROVAL
1979-06-15
LATEST ACTION
1993-03-24
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINERDiscontinued
SODIUM LACTATE 1.87GM/100ML · INJECTABLE · INJECTION

Approval history

1993-03-24Labeling · Supplement 16AP
1990-09-11Manufacturing (CMC) · Supplement 15AP
1986-02-18Manufacturing (CMC) · Supplement 10AP
1985-06-28Manufacturing (CMC) · Supplement 11AP
1985-06-24Labeling · Supplement 13AP
1985-04-03Manufacturing (CMC) · Supplement 12AP
1983-01-24Labeling · Supplement 7AP
1981-10-26Manufacturing (CMC) · Supplement 9AP
1981-02-24Manufacturing (CMC) · Supplement 8AP
1980-10-24Manufacturing (CMC) · Supplement 5AP
1980-09-25Manufacturing (CMC) · Supplement 6AP
1980-08-06Manufacturing (CMC) · Supplement 4AP
1980-02-12Manufacturing (CMC) · Supplement 3AP
1979-10-16Manufacturing (CMC) · Supplement 1AP
1979-10-09Labeling · Supplement 2AP
1979-06-15OriginalAP
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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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