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FDA NDA · NDA006135

FOLIC ACID

Sponsor: LILLY

APPLICATION
NDA006135
TYPE
NDA
ORIGINAL APPROVAL
1947-06-02
LATEST ACTION
1990-03-27
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

FOLIC ACIDDiscontinued
FOLIC ACID 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TABLET · ORAL

Approval history

1990-03-27Labeling · Supplement 8AP
1989-05-15Labeling · Supplement 6AP
1989-05-15Labeling · Supplement 7AP
1981-02-24Labeling · Supplement 5AP
1947-06-02UNKNOWN · Original · unknownAP
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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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